FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

TRIAGE PROFILER S.O.B. PANEL

K Number: K040437 · Decision Jun 25, 2004
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
56
Applicant Total
46
Review Days
127

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Basic Information

Device Name
TRIAGE PROFILER S.O.B. PANEL
K Number
K040437
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7320
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biosite Incorporated
Date Received
February 19, 2004
Decision Date
June 25, 2004
Product Code
DAP
Advisory Committee
Hematology
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control

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Other Clearances by Biosite Incorporated

K Number Device Name
K092987 INRATIO/INRATIO2 TEST STRIPS
K092048 ONE STEP EDDP (METHADONE METABOLITE) TEST STRIP
K093032 TRIAGE TOTAL 3 CONTROLS AND CALIBRATION VERIFICATION SET
K080269 TRIAGE CARDIOPROFILER AND PROFILER S.O.B. PANELS
K072892 TRIAGE TOTAL CONTROLS 5, TRIAGE TOTAL CALIBRATION VERIFICATION 5
K062840 TRIAGE PROTEIN C CONTROLS AND CALIBRATION VERIFICATION CONTROLS
K062530 TRIAGE PROTEIN C TEST
K060788 TRIAGE TOX DRUG SCREEN CONTROL LEVEL 1 MODEL 94413 AND LEVEL 2 MODEL 94414
K060791 TRIAGE TOX DRUG SCREEN, MODEL 94400
K052789 TRIAGE BNP TEST FOR BECKMAN COULTER IMMUNOASSAY SYSTEMS, MODEL 98200
Search all 46 clearances from Biosite Incorporated →