Medical Device Manufacturer · DE , Mainz

Medovent GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Medovent GmbH has 2 FDA 510(k) cleared medical devices. Based in Mainz, DE.

Historical record: 2 cleared submissions from 2015 to 2018. Primary specialty: Neurology.

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

FDA 510(k) Regulatory Record - Medovent GmbH

2 devices

1-2 of 2