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

CENTRIA FSH RIA

K Number: K792233 · Decision Jan 21, 1980
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
87
Applicant Total
69
Review Days
77

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Basic Information

Device Name
CENTRIA FSH RIA
K Number
K792233
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Union Carbide Corp.
Date Received
November 5, 1979
Decision Date
January 21, 1980
Product Code
CGJ
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
CGJ Radioimmunoassay, Follicle-Stimulating Hormone

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