URIC ACID MODEL 3P39— 510(k) K102568

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K102568 for URIC ACID MODEL 3P39, Substantially Equivalent on 2011-05-06. Applicant: Abbott Laboratories. Device class: 1.

Clearance details

Applicant: Abbott Laboratories
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 2010-09-07
Decision date: 2011-05-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irving, TX, 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.