WEISS EMERGENCY AIRWAY SYSTEM— 510(k) K790650

Name: FDA 510(k) clearance K790650
Creator: U.S. Food and Drug Administration
Published: 1979-06-27

Substantially Equivalent

Intl. Medical Devices , Ltd.

FDA 510(k) clearance K790650 for WEISS EMERGENCY AIRWAY SYSTEM, Substantially Equivalent on 1979-06-27. Applicant: Intl. Medical Devices , Ltd.. Device class: 2.

Clearance details

Applicant: Intl. Medical Devices , Ltd.
Product code: Code BWC
Device class: Class 2
Regulation: 21 CFR 868.5090
Advisory panel: Anesthesiology
Date received: 1979-04-03
Decision date: 1979-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Monroeville, PA, US

Download summary PDF View on FDA.gov ↗

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