CD-102 CARBON DIOXIDE ANALYZER/RECOR— 510(k) K833739

Name: FDA 510(k) clearance K833739
Creator: U.S. Food and Drug Administration
Published: 1983-12-16

Substantially Equivalent

Instrumentarium Corp.

FDA 510(k) clearance K833739 for CD-102 CARBON DIOXIDE ANALYZER/RECOR, Substantially Equivalent on 1983-12-16. Applicant: Instrumentarium Corp.. Device class: 2.

Clearance details

Applicant: Instrumentarium Corp.
Product code: Code CCJ
Device class: Class 2
Regulation: 21 CFR 868.1430
Advisory panel: Anesthesiology
Date received: 1983-10-25
Decision date: 1983-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tewksbury, MA, US

Download summary PDF View on FDA.gov ↗

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