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

CHOLESTEROL RAPID LIQUID REAGENT

K Number: K972853 · Decision Sep 24, 1997
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
229
Applicant Total
63
Review Days
89

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Basic Information

Device Name
CHOLESTEROL RAPID LIQUID REAGENT
K Number
K972853
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1175
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Reagents Applications, Inc.
Date Received
June 27, 1997
Decision Date
September 24, 1997
Product Code
CHH
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
CHH Enzymatic Esterase--Oxidase, Cholesterol

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K911900 RAICHEM SPIA C3 REAGENT
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K911898 RAICHEM(TM) SPIA(TM) HAPTOGLOBIN REAGENT
K905084 RAICHEM CREATINE KINASE REAGENT, OPTIMIZED UV
K905085 RAICHEM GGT REAGENT
K904175 RAICHEM (TM) SPIA (TM) - ACID GLYCOPROTEIN REAGENT
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