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

ELISA TUBE FSH TEST KIT ENZYME LINKED IMMUN. ASSAY

K Number: K920917 · Decision Mar 26, 1992
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
87
Applicant Total
14
Review Days
27

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Basic Information

Device Name
ELISA TUBE FSH TEST KIT ENZYME LINKED IMMUN. ASSAY
K Number
K920917
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bio Clinic Co.
Date Received
February 28, 1992
Decision Date
March 26, 1992
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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K921212 MIRCO ELISA HPL TEST KIT
K921211 NOW PREGNANCY TEST KIT
K920920 ELISA TUBE LH TEST KIT
K920921 ELISA TUBE PROLACTIN TEST KIT
K920918 TMB CHROMOGEN/SUBSTRATE REAGENT SET
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