Kessel Medintim GmbH is one of 507 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Kessel Medintim GmbH - FDA 510(k) Cleared Devices
Recent clearances: CAYA CONTOURED DIAPHRAGM
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.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Kessel Medintim GmbH
1 devices