URIC ACID TEST— 510(k) K864119

Substantially Equivalent

U. S. Diagnostics, Inc.

FDA 510(k) clearance K864119 for URIC ACID TEST, Substantially Equivalent on 1986-10-29. Applicant: U. S. Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: U. S. Diagnostics, Inc.
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1986-10-21
Decision date: 1986-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Luis Obispo, CA, 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.