Medical Device Manufacturer · GB , Wotton-Under-Edge

Rensihaw Plc - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Total

Cleared

Denied

Rensihaw Plc has 1 FDA 510(k) cleared medical devices. Based in Wotton-Under-Edge, GB.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Rensihaw Plc Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Rensihaw Plc

1 devices

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