AS/3 COP MODULE— 510(k) K922876

Name: FDA 510(k) clearance K922876
Creator: U.S. Food and Drug Administration
Published: 1993-07-21

Substantially Equivalent

Datex Division Instrumentarium Corp.

FDA 510(k) clearance K922876 for AS/3 COP MODULE, Substantially Equivalent on 1993-07-21. Applicant: Datex Division Instrumentarium Corp.. Device class: 2.

Clearance details

Applicant: Datex Division Instrumentarium Corp.
Product code: Code CBQ
Device class: Class 2
Regulation: 21 CFR 868.1500
Advisory panel: Anesthesiology
Date received: 1992-06-15
Decision date: 1993-07-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Helsinki, Finland, FI

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