https://www.510kdatabase.net/k760466/ 1976-08-26 monthly 0.5 https://www.510kdatabase.net/og-image/k760466-table-x-ray-rfx-classical-fda-510k.jpg K760466 - TABLE, X-RAY, RFX CLASSICAL K760466 is a FDA 510(k) cleared radiology medical device. Manufacturer: General Electric Co.. Cleared Aug 1976. https://www.510kdatabase.net/k760093/ 1976-08-23 monthly 0.5 https://www.510kdatabase.net/og-image/k760093-catheter-silicone-foley-bardex-fda-510k.jpg K760093 - CATHETER, SILICONE FOLEY (BARDEX) K760093 is a FDA 510(k) cleared gastroenterology & urology medical device. Manufacturer: C.R. Bard, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760216/ 1976-08-23 monthly 0.5 https://www.510kdatabase.net/og-image/k760216-suction-instrument-macbick-poole-tip-fda-510k.jpg K760216 - SUCTION INSTRUMENT, MACBICK POOLE TIP K760216 is a FDA 510(k) cleared general hospital medical device. Manufacturer: C.R. Bard, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760217/ 1976-08-23 monthly 0.5 https://www.510kdatabase.net/og-image/k760217-suction-instrument-macbick-dis-fraz-fda-510k.jpg K760217 - SUCTION INSTRUMENT, MACBICK DIS. FRAZ. K760217 is a FDA 510(k) cleared general hospital medical device. Manufacturer: C.R. Bard, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760253/ 1976-08-23 monthly 0.5 https://www.510kdatabase.net/og-image/k760253-tray-universal-foly-wodrainage-bag-fda-510k.jpg K760253 - TRAY, UNIVERSAL FOLY WO/DRAINAGE BAG K760253 is a FDA 510(k) cleared gastroenterology & urology medical device. Manufacturer: C.R. Bard, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760254/ 1976-08-23 monthly 0.5 https://www.510kdatabase.net/og-image/k760254-tray-foley-catheter-fda-510k.jpg K760254 - TRAY, FOLEY CATHETER K760254 is a FDA 510(k) cleared gastroenterology & urology medical device. Manufacturer: C.R. Bard, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760259/ 1976-08-23 monthly 0.5 https://www.510kdatabase.net/og-image/k760259-catheter-3-way-silicone-foley-fda-510k.jpg K760259 - CATHETER 3-WAY SILICONE FOLEY K760259 is a FDA 510(k) cleared gastroenterology & urology medical device. Manufacturer: Travenol Laboratories, S.A.. Cleared Aug 1976. https://www.510kdatabase.net/k760332/ 1976-08-23 monthly 0.5 https://www.510kdatabase.net/og-image/k760332-sigma-ammonia-reagent-fda-510k.jpg K760332 - SIGMA AMMONIA REAGENT K760332 is a FDA 510(k) cleared chemistry medical device. Manufacturer: Sigma Chemical Co.. Cleared Aug 1976. https://www.510kdatabase.net/k760277/ 1976-08-11 monthly 0.5 https://www.510kdatabase.net/og-image/k760277-underpad-code-no-8453-fda-510k.jpg K760277 - UNDERPAD CODE NO. 8453 K760277 is a FDA 510(k) cleared gastroenterology & urology medical device. Manufacturer: Johnson & Johnson Professionals, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760334/ 1976-08-11 monthly 0.5 https://www.510kdatabase.net/og-image/k760334-prostehsis-total-knee-replacement-fda-510k.jpg K760334 - PROSTEHSIS, TOTAL KNEE REPLACEMENT K760334 is a FDA 510(k) cleared orthopedic medical device. Manufacturer: Depuy, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760311/ 1976-08-09 monthly 0.5 https://www.510kdatabase.net/og-image/k760311-instruments-general-hand-surgery-fda-510k.jpg K760311 - INSTRUMENTS, GENERAL HAND & SURGERY K760311 is a FDA 510(k) cleared general & plastic surgery medical device. Manufacturer: Depuy, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760249/ 1976-08-04 monthly 0.5 https://www.510kdatabase.net/og-image/k760249-tray-sterile-disposable-arthrogram-fda-510k.jpg K760249 - TRAY, STERILE DISPOSABLE ARTHROGRAM K760249 is a FDA 510(k) cleared anesthesiology medical device. Manufacturer: Travenol Laboratories, S.A.. Cleared Aug 1976. https://www.510kdatabase.net/k760326/ 1976-08-04 monthly 0.5 https://www.510kdatabase.net/og-image/k760326-surgical-instruments-opthalmic-fda-510k.jpg K760326 - SURGICAL INSTRUMENTS, OPTHALMIC K760326 is a FDA 510(k) cleared ophthalmic medical device. Manufacturer: Depuy, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760040/ 1976-08-03 monthly 0.5 https://www.510kdatabase.net/og-image/k760040-test-mono-card-macro-vue-fda-510k.jpg K760040 - TEST, MONO., CARD (MACRO-VUE) K760040 is a FDA 510(k) cleared immunology medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Aug 1976. https://www.510kdatabase.net/k760043/ 1976-08-03 monthly 0.5 https://www.510kdatabase.net/og-image/k760043-test-rheum-arth-card-macro-vue-fda-510k.jpg K760043 - TEST, RHEUM. ARTH., CARD (MACRO-VUE) K760043 is a FDA 510(k) cleared immunology medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Aug 1976. https://www.510kdatabase.net/k760054/ 1976-08-03 monthly 0.5 https://www.510kdatabase.net/og-image/k760054-culture-tube-vacutainer-fda-510k.jpg K760054 - CULTURE TUBE, (VACUTAINER) K760054 is a FDA 510(k) cleared microbiology medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Aug 1976. https://www.510kdatabase.net/k760063/ 1976-08-03 monthly 0.5 https://www.510kdatabase.net/og-image/k760063-specimen-collector-anaerobic-fda-510k.jpg K760063 - SPECIMEN COLLECTOR, ANAEROBIC K760063 is a FDA 510(k) cleared microbiology medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Aug 1976. https://www.510kdatabase.net/k760243/ 1976-08-03 monthly 0.5 https://www.510kdatabase.net/og-image/k760243-gloves-sterile-latex-surgeons-fda-510k.jpg K760243 - GLOVES, STERILE LATEX SURGEON'S K760243 is a FDA 510(k) cleared general hospital medical device. Manufacturer: Travenol Laboratories, S.A.. Cleared Aug 1976. https://www.510kdatabase.net/k760325/ 1976-08-03 monthly 0.5 https://www.510kdatabase.net/og-image/k760325-surgical-instruments-orthopedic-fda-510k.jpg K760325 - SURGICAL INSTRUMENTS, ORTHOPEDIC K760325 is a FDA 510(k) cleared orthopedic medical device. Manufacturer: Depuy, Inc.. Cleared Aug 1976. https://www.510kdatabase.net/k760001/ 1976-07-26 monthly 0.5 https://www.510kdatabase.net/og-image/k760001-arch-support-arch-aid-fda-510k.jpg K760001 - ARCH SUPPORT (ARCH AID) K760001 is a FDA 510(k) cleared physical medicine medical device. Manufacturer: Zimmer, Inc.. Cleared Jul 1976. https://www.510kdatabase.net/k760002/ 1976-07-26 monthly 0.5 https://www.510kdatabase.net/og-image/k760002-knee-aid-fda-510k.jpg K760002 - KNEE AID K760002 is a FDA 510(k) cleared physical medicine medical device. Manufacturer: Zimmer, Inc.. Cleared Jul 1976. https://www.510kdatabase.net/k760003/ 1976-07-26 monthly 0.5 https://www.510kdatabase.net/og-image/k760003-cast-material-wicket-stockinette-fda-510k.jpg K760003 - CAST MATERIAL (WICKET STOCKINETTE) K760003 is a FDA 510(k) cleared physical medicine medical device. Manufacturer: Zimmer, Inc.. Cleared Jul 1976. https://www.510kdatabase.net/k760044/ 1976-07-26 monthly 0.5 https://www.510kdatabase.net/og-image/k760044-kit-ria-human-thyroid-hormone-fda-510k.jpg K760044 - KIT, RIA, HUMAN THYROID HORMONE K760044 is a FDA 510(k) cleared chemistry medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Jul 1976. https://www.510kdatabase.net/k760208/ 1976-07-26 monthly 0.5 https://www.510kdatabase.net/og-image/k760208-oximeter-co-il-model-282-fda-510k.jpg K760208 - OXIMETER, CO-, IL MODEL 282 K760208 is a FDA 510(k) cleared hematology medical device. Manufacturer: Instrumentation Laboratory CO. Cleared Jul 1976. https://www.510kdatabase.net/k760250/ 1976-07-26 monthly 0.5 https://www.510kdatabase.net/og-image/k760250-bandage-triangular-no-8068-fda-510k.jpg K760250 - BANDAGE, TRIANGULAR NO. 8068 K760250 is a FDA 510(k) cleared general & plastic surgery medical device. Manufacturer: Johnson & Johnson Professionals, Inc.. Cleared Jul 1976. https://www.510kdatabase.net/k760064/ 1976-07-21 monthly 0.5 https://www.510kdatabase.net/og-image/k760064-catheter-thermal-dilution-animal-ped-fda-510k.jpg K760064 - CATHETER, THERMAL DILUTION, ANIMAL & PED K760064 is a FDA 510(k) cleared cardiovascular medical device. Manufacturer: Instrumentation Laboratory CO. Cleared Jul 1976. https://www.510kdatabase.net/k760065/ 1976-07-21 monthly 0.5 https://www.510kdatabase.net/og-image/k760065-catheter-thermal-dilution-pediatric-fda-510k.jpg K760065 - CATHETER, THERMAL DILUTION, PEDIATRIC K760065 is a FDA 510(k) cleared cardiovascular medical device. Manufacturer: Instrumentation Laboratory CO. Cleared Jul 1976. https://www.510kdatabase.net/k760066/ 1976-07-21 monthly 0.5 https://www.510kdatabase.net/og-image/k760066-tray-iced-injectable-26420-fda-510k.jpg K760066 - TRAY, ICED INJECTABLE (26420) K760066 is a FDA 510(k) cleared cardiovascular medical device. Manufacturer: Instrumentation Laboratory CO. Cleared Jul 1976. https://www.510kdatabase.net/k760067/ 1976-07-21 monthly 0.5 https://www.510kdatabase.net/og-image/k760067-catheter-thermal-dilution-open-chest-fda-510k.jpg K760067 - CATHETER, THERMAL DILUTION, OPEN CHEST K760067 is a FDA 510(k) cleared cardiovascular medical device. Manufacturer: Instrumentation Laboratory CO. Cleared Jul 1976. https://www.510kdatabase.net/k760013/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760013-pacer-systems-analyzer-cordis-fda-510k.jpg K760013 - PACER SYSTEMS ANALYZER (CORDIS) K760013 is a FDA 510(k) cleared cardiovascular medical device. Manufacturer: Cordis Corp.. Cleared Jul 1976. https://www.510kdatabase.net/k760045/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760045-kit-radioassay-serum-iron-fda-510k.jpg K760045 - KIT, RADIOASSAY, SERUM IRON K760045 is a FDA 510(k) cleared chemistry medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Jul 1976. https://www.510kdatabase.net/k760118/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760118-thermometer-digital-fever-meditemp-fda-510k.jpg K760118 - THERMOMETER, DIGITAL FEVER (MEDITEMP) K760118 is a FDA 510(k) cleared general hospital medical device. Manufacturer: Johnson & Johnson Professionals, Inc.. Cleared Jul 1976. https://www.510kdatabase.net/k760119/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760119-sampler-flameless-il-model-555-fda-510k.jpg K760119 - SAMPLER, FLAMELESS (IL MODEL 555) K760119 is a FDA 510(k) cleared chemistry medical device. Manufacturer: Instrumentation Laboratory CO. Cleared Jul 1976. https://www.510kdatabase.net/k760123/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760123-autozyme-fda-510k.jpg K760123 - AUTOZYME K760123 is a FDA 510(k) cleared hematology medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Jul 1976. https://www.510kdatabase.net/k760124/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760124-auto-cell-diluent-fda-510k.jpg K760124 - AUTO CELL DILUENT K760124 is a FDA 510(k) cleared hematology medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Jul 1976. https://www.510kdatabase.net/k760131/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760131-agaro-gel-product-a1266-fda-510k.jpg K760131 - AGARO-GEL, PRODUCT # A1266 K760131 is a FDA 510(k) cleared chemistry medical device. Manufacturer: Sigma Chemical Co.. Cleared Jul 1976. https://www.510kdatabase.net/k760132/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760132-test-ria-tsh-quantimune-fda-510k.jpg K760132 - TEST, RIA, TSH QUANTIMUNE K760132 is a FDA 510(k) cleared immunology medical device. Manufacturer: Bio-Rad. Cleared Jul 1976. https://www.510kdatabase.net/k760133/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760133-procedure-red-cell-folate-assay-fda-510k.jpg K760133 - PROCEDURE, RED CELL FOLATE ASSAY K760133 is a FDA 510(k) cleared chemistry medical device. Manufacturer: Bio-Rad. Cleared Jul 1976. https://www.510kdatabase.net/k760134/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760134-procedure-ra-thyroxine-binding-protein-fda-510k.jpg K760134 - PROCEDURE, RA, THYROXINE BINDING PROTEIN K760134 is a FDA 510(k) cleared chemistry medical device. Manufacturer: Bio-Rad. Cleared Jul 1976. https://www.510kdatabase.net/k760135/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760135-test-ra-quanta-count-t-4-fda-510k.jpg K760135 - TEST, RA, QUANTA-COUNT T-4 K760135 is a FDA 510(k) cleared immunology medical device. Manufacturer: Bio-Rad. Cleared Jul 1976. https://www.510kdatabase.net/k760169/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760169-diffusion-system-single-breath-47404a-fda-510k.jpg K760169 - DIFFUSION SYSTEM, SINGLE-BREATH (47404A) K760169 is a FDA 510(k) cleared anesthesiology medical device. Manufacturer: Hewlett-Packard Co.. Cleared Jul 1976. https://www.510kdatabase.net/k760200/ 1976-07-20 monthly 0.5 https://www.510kdatabase.net/og-image/k760200-prosthesis-patellar-articular-surface-fda-510k.jpg K760200 - PROSTHESIS, PATELLAR ARTICULAR SURFACE K760200 is a FDA 510(k) cleared orthopedic medical device. Manufacturer: Depuy, Inc.. Cleared Jul 1976. https://www.510kdatabase.net/k760150/ 1976-07-19 monthly 0.5 https://www.510kdatabase.net/og-image/k760150-monitor-patient-model-78331a-fda-510k.jpg K760150 - MONITOR, PATIENT (MODEL 78331A) K760150 is a FDA 510(k) cleared cardiovascular medical device. Manufacturer: Hewlett-Packard Co.. Cleared Jul 1976. https://www.510kdatabase.net/k760160/ 1976-07-19 monthly 0.5 https://www.510kdatabase.net/og-image/k760160-monitor-patient-model-78333a-fda-510k.jpg K760160 - MONITOR, PATIENT (MODEL 78333A) K760160 is a FDA 510(k) cleared cardiovascular medical device. Manufacturer: Hewlett-Packard Co.. Cleared Jul 1976. https://www.510kdatabase.net/k760012/ 1976-07-16 monthly 0.5 https://www.510kdatabase.net/og-image/k760012-blood-warmer-code-4r4305-fda-510k.jpg K760012 - BLOOD WARMER (CODE 4R4305) K760012 is a FDA 510(k) cleared hematology medical device. Manufacturer: Travenol Laboratories, S.A.. Cleared Jul 1976. https://www.510kdatabase.net/k760039/ 1976-07-16 monthly 0.5 https://www.510kdatabase.net/og-image/k760039-valve-imv-u-mid-one-way-fda-510k.jpg K760039 - VALVE, I.M.V. (U-MID ONE WAY) K760039 is a FDA 510(k) cleared anesthesiology medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Jul 1976. https://www.510kdatabase.net/k760041/ 1976-07-16 monthly 0.5 https://www.510kdatabase.net/og-image/k760041-filter-respiratory-u-mid-fda-510k.jpg K760041 - FILTER, RESPIRATORY (U-MID) K760041 is a FDA 510(k) cleared general hospital medical device. Manufacturer: Bd Becton Dickinson Vacutainer Systems Preanalytic. Cleared Jul 1976.