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

LUQUIZYME TRIGLYCERIDE REAGENT SET

K Number: K803297 · Decision Jan 16, 1981
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
39
Review Days
17

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Basic Information

Device Name
LUQUIZYME TRIGLYCERIDE REAGENT SET
K Number
K803297
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Amresco, Inc.
Date Received
December 30, 1980
Decision Date
January 16, 1981
Product Code
CDT
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
CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

Similar 510(k) Clearances

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

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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
K903775 CREATINE PHOSPHOKINASE
K903829 AST REAGENT
Search all 39 clearances from Amresco, Inc. →