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

OLYMPUS CREATINE KINASE REAGENT OSR6179/6279

K Number: K994189 · Decision Jan 20, 2000
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
4
Review Days
38

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Basic Information

Device Name
OLYMPUS CREATINE KINASE REAGENT OSR6179/6279
K Number
K994189
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Olympus Diagnostica GmbH
Date Received
December 13, 1999
Decision Date
January 20, 2000
Product Code
CGS
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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

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Other Clearances by Olympus Diagnostica GmbH

K Number Device Name
K984145 OLYMPUS MYOGLOBIN IMMUNOTURBIDMETRIC REAGENT
K981854 OLYMPUS SERUM PROTEIN MULTICALIBRATOR,
K982035 OLYMPUS CALCIUM ARSENAZO III REAGENT