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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