Beckman Coulter Biomedical GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Beckman Coulter Biomedical GmbH - FDA 510(k) Cleared Devices
Recent clearances: DxA 5000, DxI 800 Access Immunoassay System, Access Ferritin, Access Folate, Access TSH (3rd IS), Access Vitamin B12
1
Total
1
Cleared
0
Denied
Beckman Coulter Biomedical GmbH has 1 FDA 510(k) cleared medical devices. Based in Munich, DE.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Beckman Coulter Biomedical GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Beckman Coulter Biomedical GmbH
1 devices