URIC ACID REAGENT— 510(k) K822913

Name: FDA 510(k) clearance K822913
Creator: U.S. Food and Drug Administration
Published: 1982-12-20

Substantially Equivalent

Ac Biochemical Laboratories, Inc.

FDA 510(k) clearance K822913 for URIC ACID REAGENT, Substantially Equivalent on 1982-12-20. Applicant: Ac Biochemical Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Ac Biochemical Laboratories, Inc.
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1982-10-01
Decision date: 1982-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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