KODAK RVG 6500 SYSTEM AND KODAK RVG 6500 IPS SYSTEM— 510(k) K093478

Name: FDA 510(k) clearance K093478
Creator: U.S. Food and Drug Administration
Published: 2010-04-26

Substantially Equivalent

Trophy

FDA 510(k) clearance K093478 for KODAK RVG 6500 SYSTEM AND KODAK RVG 6500 IPS SYSTEM, Substantially Equivalent on 2010-04-26. Applicant: Trophy. Device class: 2.

Clearance details

Applicant: Trophy
Product code: Code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2009-11-09
Decision date: 2010-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Croissy-Beaubourg, FR

Download summary PDF View on FDA.gov ↗

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