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

CK QVET

K Number: K950177 · Decision Mar 3, 1995
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
27
Review Days
45

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Basic Information

Device Name
CK QVET
K Number
K950177
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Prisma Systems
Date Received
January 17, 1995
Decision Date
March 3, 1995
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 Prisma Systems

K Number Device Name
K943027 CHOLESTEROL QVET
K942964 LACTATE DEHYDROGENASE QVET
K942997 ALKALINE PHOSPHATASE (ALKP) QVET
K943001 MAGNESIUM QVET
K942963 GLUCOSE QVET
K943042 BUN QVET
K944102 AST QVET
K943000 ALBUMIN QVET
K943026 POTASSIUM QVET
K943004 TOTAL PROTEIN QVET
Search all 27 clearances from Prisma Systems →