MASTERSCREEN & OXYCON CPX— 510(k) K072323

Name: FDA 510(k) clearance K072323
Creator: U.S. Food and Drug Administration
Published: 2007-10-10

Substantially Equivalent

Viasys Healthcare GmbH

FDA 510(k) clearance K072323 for MASTERSCREEN & OXYCON CPX, Substantially Equivalent on 2007-10-10. Applicant: Viasys Healthcare GmbH. Device class: 2.

Clearance details

Applicant: Viasys Healthcare GmbH
Product code: Code BZC
Device class: Class 2
Regulation: 21 CFR 868.1880
Advisory panel: Anesthesiology
Date received: 2007-08-20
Decision date: 2007-10-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Yorba Linda, CA, US

Download summary PDF View on FDA.gov ↗

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