Medical Device Manufacturer · GB , Girton

Medovate Limited - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

Medovate Limited has 1 FDA 510(k) cleared medical devices. Based in Girton, GB.

Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.

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

510(k) submissions have been managed by Delphi Medical Device Consulting, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Medovate Limited
1 devices
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