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

LABELING CHANGE COAT-A-COUNT COCAINE METABOLITE

K Number: K873751 · Decision Oct 15, 1987
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
144
Applicant Total
321
Review Days
41

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Basic Information

Device Name
LABELING CHANGE COAT-A-COUNT COCAINE METABOLITE
K Number
K873751
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3250
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Diagnostic Products Corp.
Date Received
September 4, 1987
Decision Date
October 15, 1987
Product Code
DIO
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DIO), ordered by most recent decision date.

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Other Clearances by Diagnostic Products Corp.

K Number Device Name
K063045 IMMULITE 2000, IMMULITE 2500 VANCOMYCIN
K034055 IMMULITE 2500 CK-MB, 2500 MYOGLOBIN, 2500 STAT TROPONIN I
K033234 IMMULITE 2500 AUTOMATED IMMUNOASSAY ANALYZER
K032881 IMMULITE/IMMULITE 1000 TOTAL TESTOSTERONE AND IMMULITE 2000 TOTAL TESTOSTERONE
K023152 IMMULITE 2000 ALLERGEN-SPECIFIC IGE
K023304 IMMULITE/IMMULITE 1000 CALCITONIN, MODEL LKCL AND IMMULITE 2000 CALCITONIN, MODEL L2KCL
K022603 IMMULITE 1000 AUTOMATED IMMUNOASSAY ANALYZER
K022118 IMMULITE TURBO CK-MB, MODELS LSKCP1 (100 TESTS), LSKCP5 (500 TESTS)
K021257 ANA LINE BLOT, CATALOG NUMBER: KALABI (20 TESTS)
K021208 IMMULITE 2000 MIXED ALLERGEN PANELS
Search all 321 clearances from Diagnostic Products Corp. →