CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT,— 510(k) K792047

Name: FDA 510(k) clearance K792047
Creator: U.S. Food and Drug Administration
Published: 1979-10-30

Substantially Equivalent

Airlife, Inc.

FDA 510(k) clearance K792047 for CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT,, Substantially Equivalent on 1979-10-30. Applicant: Airlife, Inc.. Device class: 1.

Clearance details

Applicant: Airlife, Inc.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1979-10-12
Decision date: 1979-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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K952011 — PRIMA BREATHING BAGS1995-05-22
K952012 — PRIMA CUSTOM ANESTESIA CIRCUIT1995-05-22

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