AS/3 COMPACT AIRWAY MODULE M-CAIOV— 510(k) K960490

Name: FDA 510(k) clearance K960490
Creator: U.S. Food and Drug Administration
Published: 1996-05-03

Substantially Equivalent

Datex Medical Instrumentation, Inc.

FDA 510(k) clearance K960490 for AS/3 COMPACT AIRWAY MODULE M-CAIOV, Substantially Equivalent on 1996-05-03. Applicant: Datex Medical Instrumentation, Inc.. Device class: 2.

Clearance details

Applicant: Datex Medical Instrumentation, Inc.
Product code: Code CBS
Device class: Class 2
Regulation: 21 CFR 868.1620
Advisory panel: Anesthesiology
Date received: 1996-02-02
Decision date: 1996-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tewksbury, MA, US

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