Kessel Medintim GmbH is one of 218 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Kessel Medintim GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kessel Medintim GmbH has 1 FDA 510(k) cleared medical devices. Based in Frankfurt, DE.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Kessel Medintim GmbH Filter by specialty or product code using the sidebar.
Kessel Medintim GmbH — FDA 510(k) Products and Clearance History
1 devices