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

PHASE II FSH KIT

K Number: K883279 · Decision Sep 9, 1988
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
87
Applicant Total
39
Review Days
37

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Basic Information

Device Name
PHASE II FSH KIT
K Number
K883279
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Vitek Systems, Inc.
Date Received
August 3, 1988
Decision Date
September 9, 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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K920952 VITEK IMMUNODIAG ASSAY SYST(VIDAS) FERRITINE ASSAY
K915884 VIDAS CHLAMYDIA ASSAY, MODIFICATION
K905211 VIDAS CLOSTRIDIUM DIFFICILE TOXIN A (CDA) ASSAY
K912371 BIOMERIEUX RSV DIRECT IF KIT
K910230 LYME-SPOT IF KIT
K910210 SLIDEX MENINGITE-KIT 5
K910304 RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIA
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