WHISTLER IN-LINE PRESSURE RELEASE VALVE— 510(k) K831246

Name: FDA 510(k) clearance K831246
Creator: U.S. Food and Drug Administration
Published: 1983-07-26

Substantially Equivalent

Airlife, Inc.

FDA 510(k) clearance K831246 for WHISTLER IN-LINE PRESSURE RELEASE VALVE, Substantially Equivalent on 1983-07-26. 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: 1983-04-18
Decision date: 1983-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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