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

BINAX FSH IRMA TEST KIT, IMMUNORADIOMETRIC ASSAY

K Number: K883305 · Decision Oct 6, 1988
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
87
Applicant Total
30
Review Days
63

Basic Information

Device Name
BINAX FSH IRMA TEST KIT, IMMUNORADIOMETRIC ASSAY
K Number
K883305
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
BINAX, INC.
Date Received
August 4, 1988
Decision Date
October 6, 1988
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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