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

CREATINE PHOSPHOKINASE

K Number: K903775 · Decision Oct 4, 1990
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
122
Applicant Total
39
Review Days
45

Basic Information

Device Name
CREATINE PHOSPHOKINASE
K Number
K903775
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
AMRESCO, INC.
Date Received
August 20, 1990
Decision Date
October 4, 1990
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 AMRESCO, INC.

K Number Device Name
K905618 GGT REAGENT
K904468 DIRECT BILIRUBIN REAGENT, 7776/7777/7576/7476/7176
K905684 ALKALINE PHOSPHATASE
K905544 MAGNESIUM REAGENT
K905284 HDL-CHOLESTEROL PRECIPITANT 7773/7573/7473/7173
K904004 AMRESCOCREAT KINASE REAGENT 7716/17,7516,7416,7116
K905096 GGT REAGENTS, 7738, 7739, 7538, 7438 & 7138
K904381 DIAZO COLORIMENTRY DIRECT BILIRUBIN
K903829 AST REAGENT
K904007 BICARBONATE REAGENTS AMRESCO PRODUCT #4326020
Search all 39 clearances from AMRESCO, INC. →