OSRAM ULTRAMED 400 W— 510(k) K863937

Name: FDA 510(k) clearance K863937
Creator: U.S. Food and Drug Administration
Published: 1986-11-04

Substantially Equivalent for Some Indications

Osram GmbH

FDA 510(k) clearance K863937 for OSRAM ULTRAMED 400 W, Substantially Equivalent for Some Indications on 1986-11-04. Applicant: Osram GmbH. Device class: 2.

Clearance details

Applicant: Osram GmbH
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1986-10-09
Decision date: 1986-11-04
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: West Germany, DE

Download summary PDF View on FDA.gov ↗

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