CAPNOMAC ULTIMA ANESTHESIA MONITOR— 510(k) K905754

Name: FDA 510(k) clearance K905754
Creator: U.S. Food and Drug Administration
Published: 1991-06-17

Substantially Equivalent

Datex Division Instrumentarium Corp.

FDA 510(k) clearance K905754 for CAPNOMAC ULTIMA ANESTHESIA MONITOR, Substantially Equivalent on 1991-06-17. Applicant: Datex Division Instrumentarium Corp.. Device class: 2.

Clearance details

Applicant: Datex Division Instrumentarium Corp.
Product code: Code CBS
Device class: Class 2
Regulation: 21 CFR 868.1620
Advisory panel: Anesthesiology
Date received: 1990-12-24
Decision date: 1991-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Helsinki, Finland, FI

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