OXYCARE(TM) OXYGEN CONTROLLER/MONITOR— 510(k) K924679

Name: FDA 510(k) clearance K924679
Creator: U.S. Food and Drug Administration
Published: 1995-02-21

Substantially Equivalent

Air-Shields Vickers, Inc.

FDA 510(k) clearance K924679 for OXYCARE(TM) OXYGEN CONTROLLER/MONITOR, Substantially Equivalent on 1995-02-21. Applicant: Air-Shields Vickers, Inc.. Device class: 2.

Clearance details

Applicant: Air-Shields Vickers, Inc.
Product code: Code KLK
Device class: Class 2
Regulation: 21 CFR 868.2500
Advisory panel: Anesthesiology
Date received: 1992-09-16
Decision date: 1995-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hatboro, PA, US

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