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

COLORIMETRIC URIC ACID REAGENT SET

K Number: K820632 · Decision Mar 25, 1982
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
117
Applicant Total
11
Review Days
17

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Basic Information

Device Name
COLORIMETRIC URIC ACID REAGENT SET
K Number
K820632
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1775
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biorent Diagnostic, Inc.
Date Received
March 8, 1982
Decision Date
March 25, 1982
Product Code
KNK
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
KNK Acid, Uric, Uricase (Colorimetric)

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Other Clearances by Biorent Diagnostic, Inc.

K Number Device Name
K832747 ALBUMIN REAGENT SET
K823060 HEMOGLOBIN REAGENT
K823211 CK-UV REAGENT
K822494 OPTIMIZED UV-GPT REAGENT SET
K822493 OPTIMIZED UV-GOT REAGENT SET
K822492 OPTIMIZED UV-LDH REAGENT SET
K820768 COLORIMETRIC LDH REAGENT SET
K813555 GLUCOSE ENZYME-COLOR REAGENT SET
K813244 UV URIC ACID DETERMINATION
K811760 CHOLESTEROL DETERMINATION
Search all 11 clearances from Biorent Diagnostic, Inc. →