Medical Device Manufacturer · DE , Rastatt

Maquet GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2018

Total

Cleared

Denied

Maquet GmbH has 3 FDA 510(k) cleared medical devices. Based in Rastatt, DE.

Last cleared in 2022. Active since 2018. Primary specialty: General Hospital.

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

FDA 510(k) cleared devices by Maquet GmbH

3 devices

1-3 of 3