UTAK LABORATORIES TOXICOLOGY CONTROL— 510(k) K903061

Name: FDA 510(k) clearance K903061
Creator: U.S. Food and Drug Administration
Published: 1991-04-12

Substantially Equivalent

Utak Laboratories, Inc.

FDA 510(k) clearance K903061 for UTAK LABORATORIES TOXICOLOGY CONTROL, Substantially Equivalent on 1991-04-12. Applicant: Utak Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Utak Laboratories, Inc.
Product code: Code LAS
Device class: Class 1
Regulation: 21 CFR 862.3280
Advisory panel: Clinical Toxicology
Date received: 1990-07-09
Decision date: 1991-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canyon Country, CA, US

Download summary PDF View on FDA.gov ↗

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