Primum Hydrophilic Guiding Catheter
Jun 2025
90d
Pendracare
1
Total
1
Cleared
0
Denied
Pendracare — FDA 510(k) Submissions
Pendracare has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Catheter, Percutaneous . Use the specialty filter in the sidebar to narrow results.
1 devices