ONE-WAY VALVE— 510(k) K790151

Substantially Equivalent

Airlife, Inc.

FDA 510(k) clearance K790151 for ONE-WAY VALVE, Substantially Equivalent on 1979-03-12. Applicant: Airlife, Inc.. Device class: 2.

Clearance details

Applicant: Airlife, Inc.
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 1979-01-12
Decision date: 1979-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Airlife, Inc.

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Data sourced from openFDA. This site is unofficial and independent of the FDA.