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

COAT-A-COUNT T3 RIA KIT

K Number: K812246 · Decision Aug 20, 1981
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
321
Review Days
9

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Basic Information

Device Name
COAT-A-COUNT T3 RIA KIT
K Number
K812246
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Diagnostic Products Corp.
Date Received
August 11, 1981
Decision Date
August 20, 1981
Product Code
CDP
Advisory Committee
Clinical Chemistry
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
CDP Radioimmunoassay, Total Triiodothyronine

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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. →