3D VIDEO SYSTEM— 510(k) K934883

Name: FDA 510(k) clearance K934883
Creator: U.S. Food and Drug Administration
Published: 1994-03-07

Substantially Equivalent

Richard Wolf Medical Instruments Corp.

FDA 510(k) clearance K934883 for 3D VIDEO SYSTEM, Substantially Equivalent on 1994-03-07. Applicant: Richard Wolf Medical Instruments Corp.. Device class: 1.

Clearance details

Applicant: Richard Wolf Medical Instruments Corp.
Product code: Code FWG
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1993-10-12
Decision date: 1994-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vernon Hills, IL, US

Download summary PDF View on FDA.gov ↗

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