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

OPTIMIZED UV-GOT REAGENT SET

K Number: K822493 · Decision Sep 21, 1982
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
138
Applicant Total
11
Review Days
34

Basic Information

Device Name
OPTIMIZED UV-GOT REAGENT SET
K Number
K822493
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1100
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
BIORENT DIAGNOSTIC, INC.
Date Received
August 18, 1982
Decision Date
September 21, 1982
Product Code
CIT
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
CIT Nadh Oxidation/Nad Reduction, Ast/Sgot

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Other Clearances by BIORENT DIAGNOSTIC, INC.

K Number Device Name
K832747 ALBUMIN REAGENT SET
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K823060 HEMOGLOBIN REAGENT
K822494 OPTIMIZED UV-GPT REAGENT SET
K822492 OPTIMIZED UV-LDH REAGENT SET
K820768 COLORIMETRIC LDH REAGENT SET
K820632 COLORIMETRIC URIC ACID REAGENT SET
K813555 GLUCOSE ENZYME-COLOR REAGENT SET
K813244 UV URIC ACID DETERMINATION
K811760 CHOLESTEROL DETERMINATION
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