MASTERSCREEN PFT BODY— 510(k) K951901

Name: FDA 510(k) clearance K951901
Creator: U.S. Food and Drug Administration
Published: 1995-07-31

Substantially Equivalent

Erich Jaeger GmbH & Co. KG

FDA 510(k) clearance K951901 for MASTERSCREEN PFT BODY, Substantially Equivalent on 1995-07-31. Applicant: Erich Jaeger GmbH & Co. KG. Device class: 2.

Clearance details

Applicant: Erich Jaeger GmbH & Co. KG
Product code: Code JEH
Device class: Class 2
Regulation: 21 CFR 868.1760
Advisory panel: Anesthesiology
Date received: 1995-04-24
Decision date: 1995-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hoechberg, DE

Download summary PDF View on FDA.gov ↗

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