Medical Device Manufacturer · US , Torrance , CA

Sakura Finetek U.S.A., Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1988

Total

Cleared

Denied

Sakura Finetek U.S.A., Inc. has 4 FDA 510(k) cleared medical devices. Based in Torrance, US.

Historical record: 4 cleared submissions from 1988 to 1989. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Sakura Finetek U.S.A., Inc.

4 devices

1-4 of 4