Precision Dynamics Corp. is one of 13352 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Dynamics Corp. - FDA 510(k) Cleared Devices
Recent clearances: SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE, SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565, SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540
25
Total
24
Cleared
0
Denied
Precision Dynamics Corp. has 24 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 24 cleared submissions from 1977 to 2002. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Precision Dynamics Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Precision Dynamics Corp.
25 devices
Cleared
Jun 03, 2002
SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE
Obstetrics & Gynecology
90d
Cleared
Mar 22, 2000
SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565
Obstetrics & Gynecology
90d
Cleared
Jan 24, 2000
SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540
Obstetrics & Gynecology
38d
Cleared
Apr 06, 1999
'ECURLINE UMBILICAL CORD CLAMP #3500
Obstetrics & Gynecology
32d
Cleared
Nov 01, 1988
PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEM
Microbiology
15d
Cleared
Jul 08, 1988
MECHANICAL CHANGE IN IN-VITRO MICRO DEVICE
Microbiology
17d
Cleared
Jan 20, 1988
SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY
General & Plastic Surgery
68d
Cleared
Oct 20, 1987
SECURLINE FRANSEENE NEEDLE
Gastroenterology & Urology
60d
Cleared
Jul 09, 1987
PRECISION CULTURE C.A.T.S. COLLECT/TRANS HSV I/II
Microbiology
15d
Cleared
Aug 27, 1986
AGAR REDUCTION IN FORMULA FOR PDC 110 & 310 MEDIA
Microbiology
9d
Cleared
Apr 22, 1985
FRANZEN NEEDLE GUIDE FOR TRANSRECTAL PROSTATE BIOP
Gastroenterology & Urology
18d
Cleared
Jan 30, 1985
PDC 104 & PDC 304 STYLE CULTURE COLLECTION & TRANS
Microbiology
64d