TOYO JOZO URIC ACID TEST— 510(k) K842103

Name: FDA 510(k) clearance K842103
Creator: U.S. Food and Drug Administration
Published: 1984-08-12

Substantially Equivalent

Advocacy International, Ltd.

FDA 510(k) clearance K842103 for TOYO JOZO URIC ACID TEST, Substantially Equivalent on 1984-08-12. Applicant: Advocacy International, Ltd.. Device class: 1.

Clearance details

Applicant: Advocacy International, Ltd.
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1984-05-25
Decision date: 1984-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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