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

FSH ENZYME IMMUNASSAY TEST KIT NO:KIF4057

K Number: K915208 · Decision Dec 18, 1991
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
87
Applicant Total
39
Review Days
30

Basic Information

Device Name
FSH ENZYME IMMUNASSAY TEST KIT NO:KIF4057
K Number
K915208
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
MEDIX BIOTECH, INC.
Date Received
November 18, 1991
Decision Date
December 18, 1991
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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