Medical Device Manufacturer · US , Waltham , MA

Fujifilm New Development U.S.A., Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2017

Total

Cleared

Denied

Fujifilm New Development U.S.A., Inc. has 3 FDA 510(k) cleared medical devices. Based in Waltham, US.

Historical record: 3 cleared submissions from 2017 to 2018. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Fujifilm New Development U.S.A., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Fujifilm New Development U.S.A., Inc.

3 devices

1-3 of 3