Medical Device Manufacturer · US , Washington , DC

Fujinon, Inc. - FDA 510(k) Cleared Devices

30 submissions · 30 cleared · Since 1990

Recent clearances: FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EG-530UR2 AND EG-530UT2, FUJINON COLONOSCOPES, FUJINON EPX-4440HD DIGITAL VIDEO PROCESSOR

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.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Fujinon, Inc.

30 devices
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