ARTEC TWIST VALVE— 510(k) K830056

Name: FDA 510(k) clearance K830056
Creator: U.S. Food and Drug Administration
Published: 1983-03-09

Substantially Equivalent

Artec Environmental Monitoring Division

FDA 510(k) clearance K830056 for ARTEC TWIST VALVE, Substantially Equivalent on 1983-03-09. Applicant: Artec Environmental Monitoring Division. Device class: 1.

Clearance details

Applicant: Artec Environmental Monitoring Division
Product code: Code BTC
Device class: Class 1
Regulation: 21 CFR 868.5320
Advisory panel: Anesthesiology
Date received: 1983-01-06
Decision date: 1983-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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