Fluobeam 800 Clinic Imaging Device used with Fluocase 800 Control System— 510(k) DEN170092

Name: FDA 510(k) clearance DEN170092
Creator: U.S. Food and Drug Administration
Published: 2018-11-02

Unknown

Fluoptics

FDA 510(k) clearance DEN170092 for Fluobeam 800 Clinic Imaging Device used with Fluocase 800 Control System, Unknown on 2018-11-02. Applicant: Fluoptics. Device class: 2.

Clearance details

Applicant: Fluoptics
Product code: Code QDG
Device class: Class 2
Regulation: 21 CFR 878.4550
Advisory panel: General, Plastic Surgery
Date received: 2017-12-22
Decision date: 2018-11-02
Decision: Unknown
Clearance type: Direct
Location: Grenoble Cedex 9, FR

View on FDA.gov ↗

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