AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE— 510(k) K923433

Name: FDA 510(k) clearance K923433
Creator: U.S. Food and Drug Administration
Published: 1993-07-22

Substantially Equivalent

Instrumentarium Corp.

FDA 510(k) clearance K923433 for AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE, Substantially Equivalent on 1993-07-22. Applicant: Instrumentarium Corp.. Device class: 2.

Clearance details

Applicant: Instrumentarium Corp.
Product code: Code CBQ
Device class: Class 2
Regulation: 21 CFR 868.1500
Advisory panel: Anesthesiology
Date received: 1992-07-13
Decision date: 1993-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Finland, FI

Download summary PDF View on FDA.gov ↗

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