MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY— 510(k) K072061

Name: FDA 510(k) clearance K072061
Creator: U.S. Food and Drug Administration
Published: 2008-04-22

Substantially Equivalent

Viasys Healthcare GmbH

FDA 510(k) clearance K072061 for MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY, Substantially Equivalent on 2008-04-22. Applicant: Viasys Healthcare GmbH. Device class: 2.

Clearance details

Applicant: Viasys Healthcare GmbH
Product code: Code JEH
Device class: Class 2
Regulation: 21 CFR 868.1760
Advisory panel: Anesthesiology
Date received: 2007-07-27
Decision date: 2008-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Yorba Linda, CA, US

Download summary PDF View on FDA.gov ↗

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