Medical Device Manufacturer · JP , Tokyo

Denka Seiken'S - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1998

Total

Cleared

Denied

Denka Seiken'S has 4 FDA 510(k) cleared medical devices. Based in Tokyo, JP.

Historical record: 4 cleared submissions from 1998 to 2002. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Denka Seiken'S Filter by specialty or product code using the sidebar.

4 devices

1–4 of 4