Bruker Daltonik GmbH is one of 387 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Bruker Daltonik GmbH - FDA 510(k) Cleared Devices
Recent clearances: MBT Sepsityper, MALDI Biotyper CA (MBT-CA) System, MBT smart CA System
3
Total
2
Cleared
1
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.
510(k) submissions have been managed by Bruker Daltonics, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Bruker Daltonik GmbH
3 devices