Medical Device Manufacturer · US , Torrance , CA

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

4 submissions · 4 cleared · Since 1988
4
Total
4
Cleared
0
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.

4 devices
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