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

SHBG IRMA KIT

K Number: K905247 · Decision Jan 17, 1991
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
88
Applicant Total
82
Review Days
57

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Basic Information

Device Name
SHBG IRMA KIT
K Number
K905247
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1680
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Ventrex Laboratories, Inc.
Date Received
November 21, 1990
Decision Date
January 17, 1991
Product Code
CDZ
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
CDZ Radioimmunoassay, Testosterones And Dihydrotestosterone

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K914554 SPECIFIC IGE EIA-TURBO ASSAY
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K913434 VENTREX COATED TUBE INTACT PTH
K905612 VENTREX COATED TUBE IGE RADIOIMMUNOASSAY
K905636 VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY
K904330 TURBO-RAST SPECIFIC IGE ASSAY
K903000 TURBO-RAST SPECIFIC IGE ASSAY
K897083 VENTRESIGN STREP A TEST
K895648 COATED TUBE HIGH SENSITIVITY TSH 100 UIU/ML STAN.
K895649 COATED TUBE HIGH SENSITIVITY TSH 200 UIU/ML STAN.
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