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

ALBUMIN REAGENT SET

K Number: K832747 · Decision Oct 14, 1983
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
119
Applicant Total
11
Review Days
60

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Basic Information

Device Name
ALBUMIN REAGENT SET
K Number
K832747
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1035
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biorent Diagnostic, Inc.
Date Received
August 15, 1983
Decision Date
October 14, 1983
Product Code
CIX
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
CIX Bromcresol Green Dye-Binding, Albumin

Similar 510(k) Clearances

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Other Clearances by Biorent Diagnostic, Inc.

K Number Device Name
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
K820632 COLORIMETRIC URIC ACID REAGENT SET
K813555 GLUCOSE ENZYME-COLOR REAGENT SET
K813244 UV URIC ACID DETERMINATION
K811760 CHOLESTEROL DETERMINATION
Search all 11 clearances from Biorent Diagnostic, Inc. →