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

GAMMA COAT ASSAY TESTOSTERONE RADIOIMMUNOASSAY KIT

K Number: K915570 · Decision Jan 27, 1992
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
88
Applicant Total
58
Review Days
46

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Basic Information

Device Name
GAMMA COAT ASSAY TESTOSTERONE RADIOIMMUNOASSAY KIT
K Number
K915570
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1680
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Incstar Corp.
Date Received
December 12, 1991
Decision Date
January 27, 1992
Product Code
CDZ
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
CDZ Radioimmunoassay, Testosterones And Dihydrotestosterone

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K960367 INCSTAR RUBELLA IGG ELISA ASSAY
K960358 INCSTAR RUBELLA IGG FAST ELISA ASSAY
K960434 INCSTAR CYTOMEGALOVIRUS IGM CAPTURE ELISA ASSAY MODEL 8530
K953567 INCSTAR 25-HYDROXYVITMIN D 1251 RIA
K955362 INCSTAR HSV I/II IGG FAST ELISA ASSAY
K955363 INCSTAR HSZ I/II IGG ELISA ASSAY
K955361 INCSTAR CYTOMEGALOVIRUS IGG ELISA ASSAY
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