Medical Device Manufacturer · DE , Bremen

Bruker Daltonik GmbH - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 2017

Total

Cleared

Denied

Bruker Daltonik GmbH has 2 FDA 510(k) cleared medical devices. Based in Bremen, DE.

Historical record: 2 cleared submissions from 2017 to 2020. Primary specialty: Microbiology.

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

FDA 510(k) cleared devices by Bruker Daltonik GmbH

3 devices

1-3 of 3