Medical Device Manufacturer · US , Washington , DC

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

30 submissions · 30 cleared · Since 1990
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.

FDA 510(k) Regulatory Record - Fujinon, Inc.
30 devices
1-12 of 30
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