QAC CONTROL— 510(k) K812950

Name: FDA 510(k) clearance K812950
Creator: U.S. Food and Drug Administration
Published: 1981-12-17

Substantially Equivalent

The Quality Assurance Service Corp.

FDA 510(k) clearance K812950 for QAC CONTROL, Substantially Equivalent on 1981-12-17. Applicant: The Quality Assurance Service Corp.. Device class: 1.

Clearance details

Applicant: The Quality Assurance Service Corp.
Product code: Code DIF
Device class: Class 1
Regulation: 21 CFR 862.3280
Advisory panel: Clinical Toxicology
Date received: 1981-10-21
Decision date: 1981-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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