ANESTHETIC GAS MONITOR TYPE 1304, MODIFIED— 510(k) K914295

Name: FDA 510(k) clearance K914295
Creator: U.S. Food and Drug Administration
Published: 1992-04-10

Substantially Equivalent

Bruel & Kjaer

FDA 510(k) clearance K914295 for ANESTHETIC GAS MONITOR TYPE 1304, MODIFIED, Substantially Equivalent on 1992-04-10. Applicant: Bruel & Kjaer. Device class: 2.

Clearance details

Applicant: Bruel & Kjaer
Product code: Code CBQ
Device class: Class 2
Regulation: 21 CFR 868.1500
Advisory panel: Anesthesiology
Date received: 1991-09-09
Decision date: 1992-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naerum 2850, DK

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