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.

Bruker Daltonik GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Bruker Daltonik GmbH

3 devices

1-3 of 3