Fresenius Kabi Deutschland GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Fresenius Kabi Deutschland GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Fresenius Kabi Deutschland GmbH has 1 FDA 510(k) cleared medical devices. Based in Bad Homburg, DE.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Fresenius Kabi Deutschland GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fresenius Kabi Deutschland GmbH
1 devices