RocaTub Ureteral Catheter
Apr 2020
255d
Promepal Sam
1
Total
1
Cleared
0
Denied
Promepal Sam — FDA 510(k) Submissions
Promepal Sam has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Catheter, Ureteral, Gastro-urology . Use the specialty filter in the sidebar to narrow results.
1 devices