Biosite Incorporated - FDA 510(k) Cleared Devices
46
Total
45
Cleared
1
Denied
Biosite Incorporated has 45 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 45 cleared submissions from 1990 to 2010. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Biosite Incorporated Filter by specialty or product code using the sidebar.
46 devices
Cleared
Jun 11, 2010
INRATIO/INRATIO2 TEST STRIPS
Hematology
256d
Cleared
Apr 19, 2010
ONE STEP EDDP (METHADONE METABOLITE) TEST STRIP
Chemistry
286d
Cleared
Nov 13, 2009
TRIAGE TOTAL 3 CONTROLS AND CALIBRATION VERIFICATION SET
Chemistry
45d
Cleared
Jun 06, 2008
TRIAGE CARDIOPROFILER AND PROFILER S.O.B. PANELS
Chemistry
126d
Cleared
Dec 07, 2007
TRIAGE TOTAL CONTROLS 5, TRIAGE TOTAL CALIBRATION VERIFICATION 5
Chemistry
58d
Cleared
Mar 01, 2007
TRIAGE PROTEIN C CONTROLS AND CALIBRATION VERIFICATION CONTROLS
Hematology
160d
Cleared
Jan 29, 2007
TRIAGE PROTEIN C TEST
Hematology
153d
Cleared
Jul 10, 2006
TRIAGE TOX DRUG SCREEN CONTROL LEVEL 1 MODEL 94413 AND LEVEL 2 MODEL 94414
Chemistry
109d
Cleared
Jun 22, 2006
TRIAGE TOX DRUG SCREEN, MODEL 94400
Toxicology
91d
Cleared
Jan 23, 2006
TRIAGE BNP TEST FOR BECKMAN COULTER IMMUNOASSAY SYSTEMS, MODEL 98200
Chemistry
112d
Cleared
Sep 22, 2005
TRIAGE BNP TEST, MODEL 98000XR
Chemistry
83d
Cleared
Jun 29, 2005
TRIAGE(R) D-DIMER CALIBRATION VERIFICATION CONTROLS
Hematology
91d
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