Fujifilm Medical Systems U.S.A, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FUJIFILM Bronchoscope Model EB-530P, FUJIFILM Ultrasonic Processor SP-900 and FUJIFILM Ultrasonic Probe PB2020-M
39
Total
39
Cleared
0
Denied
FDA 510(k) Regulatory Record - Fujifilm Medical Systems U.S.A, Inc. Ear, Nose, Throat ✕
1 devices