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FDA 510(k) Applications Submitted by FLUOPTICS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K132475
08/07/2013
FLUOBEAM 800 CLINIC LASER IMAGING DEVICE AND FLUOCASE 800 CONTROL SYSTEM
FLUOPTICS
DEN170092
12/22/2017
Fluobeam 800 Clinic Imaging Device used with Fluocase 800 Control System
Fluoptics
K190891
04/05/2019
Fluobeam LX
Fluoptics
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