TOXICOLOGY CONTROL— 510(k) K810201

Substantially Equivalent

Utak Laboratories, Inc.

FDA 510(k) clearance K810201 for TOXICOLOGY CONTROL, Substantially Equivalent on 1981-02-04. 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: 1981-01-23
Decision date: 1981-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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