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

ENZYMATIC GLUCOSE DETERMINATION

K Number: K823474 · Decision Dec 30, 1982
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
400
Applicant Total
26
Review Days
38

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Basic Information

Device Name
ENZYMATIC GLUCOSE DETERMINATION
K Number
K823474
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
The Dow Chemical Co.
Date Received
November 22, 1982
Decision Date
December 30, 1982
Product Code
CGA
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
CGA Glucose Oxidase, Glucose

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K Number Device Name
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K820675 BILIRUBIN(TOTAL) DETERMINATION CTMS
K820714 DOW BILIRUBIN(DIRECT) DETERMINATION
K812777 DIRECT IRON REAGENT SET
K811806 QUICK-CHEM COLORIMETER
K810861 CREATINE KINASE MB ISOENZYME IMMUNO UV
K810727 AST-UV (PLP-ACTIVATED) DETERMINATION
K801501 UV URIC ACID STANDARDS
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