CAYA CONTOURED DIAPHRAGM
Aug 2014
200d
Kessel Medintim GmbH
1
Total
1
Cleared
0
Denied
Kessel Medintim GmbH — FDA 510(k) Submissions
Kessel Medintim GmbH has submitted 1 FDA 510(k) premarket notifications since 2014, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Diaphragm, Contraceptive (and Accessories) . Use the specialty filter in the sidebar to narrow results.
1 devices