Medical Device Manufacturer · FR , Montpellier

Medtech S.A - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2009

Total

Cleared

Denied

Medtech S.A has 8 FDA 510(k) cleared medical devices. Based in Montpellier, FR.

Historical record: 8 cleared submissions from 2009 to 2020. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Medtech S.A

8 devices

1-8 of 8