Medical Device Manufacturer · DE , Munich

Livanova Deutschland, GmbH - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2020

Total

Cleared

Denied

Livanova Deutschland, GmbH has 7 FDA 510(k) cleared medical devices. Based in Munich, DE.

Last cleared in 2023. Active since 2020. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Livanova Deutschland, GmbH

7 devices

1-7 of 7