Fujifilm Medical System U.S.A., Inc. - FDA 510(k) Cleared Devices

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.

Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Regulatory Technology Services, LLC.