CORRUGATED FLEXIBLE E.V.A. TUBING— 510(k) K790159

Name: FDA 510(k) clearance K790159
Creator: U.S. Food and Drug Administration
Published: 1979-02-08

Substantially Equivalent

Airlife, Inc.

FDA 510(k) clearance K790159 for CORRUGATED FLEXIBLE E.V.A. TUBING, Substantially Equivalent on 1979-02-08. Applicant: Airlife, Inc.. Device class: 1.

Clearance details

Applicant: Airlife, Inc.
Product code: Code BYX
Device class: Class 1
Regulation: 21 CFR 868.5860
Advisory panel: Anesthesiology
Date received: 1979-01-12
Decision date: 1979-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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