FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TESTOSTERONE RIA KIT (125I)

K Number: K772191 · Decision Jan 12, 1978
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
88
Applicant Total
321
Review Days
48

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Basic Information

Device Name
TESTOSTERONE RIA KIT (125I)
K Number
K772191
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1680
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Diagnostic Products Corp.
Date Received
November 25, 1977
Decision Date
January 12, 1978
Product Code
CDZ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
CDZ Radioimmunoassay, Testosterones And Dihydrotestosterone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CDZ), 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. →