Fresenius Kabi Deutschland GmbH is one of 507 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
Recent clearances: COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS
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.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Fresenius Kabi Deutschland GmbH
1 devices