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

GLUCOSE QVET

K Number: K942963 · Decision Dec 29, 1994
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
142
Applicant Total
27
Review Days
189

Basic Information

Device Name
GLUCOSE QVET
K Number
K942963
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PRISMA SYSTEMS
Date Received
June 23, 1994
Decision Date
December 29, 1994
Product Code
CFR
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
CFR Hexokinase, Glucose

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CFR), ordered by most recent decision date.

View all

Other Clearances by PRISMA SYSTEMS

K Number Device Name
K950177 CK QVET
K943027 CHOLESTEROL QVET
K943001 MAGNESIUM QVET
K943042 BUN QVET
K942997 ALKALINE PHOSPHATASE (ALKP) QVET
K942964 LACTATE DEHYDROGENASE QVET
K943000 ALBUMIN QVET
K944102 AST QVET
K943026 POTASSIUM QVET
K943004 TOTAL PROTEIN QVET
Search all 27 clearances from PRISMA SYSTEMS →