Eppendorf AG is one of 491 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Eppendorf AG - FDA 510(k) Cleared Devices
Recent clearances: TransferMan 4m Micromanipulator
1
Total
1
Cleared
0
Denied
Eppendorf AG has 1 FDA 510(k) cleared medical devices. Based in Hamburg, DE.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Eppendorf AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aptiv Solutions as regulatory consultant.
FDA 510(k) Regulatory Record - Eppendorf AG
1 devices