Medical Device Manufacturer · GB , Uxbridge

Intervene Group Limited - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Total

Cleared

Denied

Intervene Group Limited has 1 FDA 510(k) cleared medical devices. Based in Uxbridge, GB.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Intervene Group Limited Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Intervene Group Limited

1 devices

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