Fujinon, Inc. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
Fujinon, Inc. has 30 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 30 cleared submissions from 1990 to 2012. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Fujinon, Inc. Filter by specialty or product code using the sidebar.
30 devices
Cleared
Aug 13, 2012
FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EG-530UR2 AND EG-530UT2
Radiology
181d
Cleared
Jul 26, 2012
FUJINON COLONOSCOPES
Gastroenterology & Urology
342d
Cleared
May 25, 2011
FUJINON EPX-4440HD DIGITAL VIDEO PROCESSOR
Gastroenterology & Urology
268d
Cleared
May 16, 2011
FUJINON ULTRASONIC PROCESSOR
Radiology
13d
Cleared
Aug 07, 2009
FUJINON STERILE OVERTUBES
Gastroenterology & Urology
52d
Cleared
Apr 22, 2009
FUJINON COLONOSCOPE FOR DOUBLE BALLOON ENTERSCOPY SYSTEM MODEL, EC-450B15
Gastroenterology & Urology
91d
Cleared
Mar 16, 2007
FUJINON MODEL EG-530N TRANS NASAL INSERTION
Gastroenterology & Urology
134d
Cleared
Mar 01, 2007
FUJINON ULTRASONIC ENDOSCOPE AND PROCESSOR, MODELS EG-530UR, EG-530UT AND SU-700
Radiology
64d
Cleared
May 19, 2005
FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P
Ear, Nose, Throat
38d
Cleared
Nov 24, 2004
FUJINON INC. G5 GASTROSCOPES, MODELS EC-450WR5, EC-250WR5
Gastroenterology & Urology
118d
Cleared
Nov 18, 2004
FUJINON G5 DUODENSCOPES
Gastroenterology & Urology
108d
Cleared
Nov 10, 2004
FUJINON G5 COLONOSCOPES, MODELS EC-450HL5 AND EC-250HL5
Gastroenterology & Urology
119d