OLYMPUS URIC ACID REAGENT— 510(k) K955752

Name: FDA 510(k) clearance K955752
Creator: U.S. Food and Drug Administration
Published: 1996-01-31

Substantially Equivalent

Olympus America, Inc.

FDA 510(k) clearance K955752 for OLYMPUS URIC ACID REAGENT, Substantially Equivalent on 1996-01-31. Applicant: Olympus America, Inc.. Device class: 1.

Clearance details

Applicant: Olympus America, Inc.
Product code: Code CDO
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1995-12-19
Decision date: 1996-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melville, NY, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.