FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ENZYMUNE-TEST TSH

K Number: K832823 · Decision Oct 14, 1983
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
48
Review Days
56

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Basic Information

Device Name
ENZYMUNE-TEST TSH
K Number
K832823
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Icl Scientific
Date Received
August 19, 1983
Decision Date
October 14, 1983
Product Code
JLW
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
JLW Radioimmunoassay, Thyroid-Stimulating Hormone

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K831383 EVENT-TEST SLIDE
K823199 ENZYME-TEST DIGOXIN
K822346 HISTIMUNE ENZYME-ANA TEST
K822777 THERAPEUTIC DRUG CONTROL
K822465 ENZYMUNE SYSTEM I
K821374 ENZYMUNE-TEST INSULIN
K821097 SYSTEMIC LUPUS ERYTHERMATOSUS ANTI-N-DNA
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