Fuji Systems Corporation - FDA 510(k) Cleared Devices

Fuji Systems Corporation has 1 FDA 510(k) cleared medical devices. Based in Nishi Shirakawa Gun, JP.

Last cleared in 2022. Active since 2022. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Fuji Systems Corporation Filter by specialty or product code using the sidebar.

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