Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Bruker Daltonik GmbH

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest FDA decision2020-12-27
TypeNumberDevice NameCodeDateActions
510(k) K193419 MBT SepsityperQNJ2020-12-27 View
510(k) K163536 MALDI Biotyper CA (MBT-CA) System, MBT smart CA SystemPEX2017-07-26 View