Fujifilm Medical System U.S.A., Inc. - FDA 510(k) Cleared Devices
71
Total
71
Cleared
0
Denied
Fujifilm Medical System U.S.A., Inc. has 71 FDA 510(k) cleared radiology devices. Based in Stamford, US.
Historical record: 71 cleared submissions from 1988 to 2017.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
71 devices
Cleared
Apr 25, 2017
Processor VP-7000, Light Source BL-7000
Gastroenterology & Urology
119d
Cleared
Mar 03, 2016
Fujifilm Ultrasonic Processors SU-1 PLATINUM and SU-1
Gastroenterology & Urology
119d
Cleared
Feb 18, 2016
Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter)
Gastroenterology & Urology
262d
Cleared
Nov 05, 2015
FDR D-EVO GL Flat Panel Detector System
Radiology
97d
Cleared
Oct 01, 2015
EPX-4440HD and EPX-4400HD with FICE
Gastroenterology & Urology
244d
Cleared
May 14, 2015
EG-530CT, EG-530D, EC-530DL, and ES-530WE Endoscopes
Gastroenterology & Urology
240d
Cleared
Oct 21, 2014
FDR D-EVO II FLAT PANEL DETECTOR SYSTEM
Radiology
90d
Cleared
Sep 09, 2014
FUJIFILM ENDOSCOPIC CO2 REGULATOR
Gastroenterology & Urology
257d
Cleared
Oct 25, 2013
MAMMOGRAPHY VIEWER SMV658
Radiology
102d
Cleared
Jun 14, 2013
SYNAPSE 3D LUNG AND ABDOMEN ANALYSIS
Radiology
105d
Cleared
Apr 09, 2013
SYNAPSE 3D CARDIAC TOOLS
Radiology
54d
Cleared
Dec 13, 2012
FUJINON/FUJIFILM EB-530 SERIES BRONCHOSCOPES (EB-530S, EB-530T AND EB-530H
Ear, Nose, Throat
115d
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