Convatec - FDA 510(k) Cleared Devices
Recent clearances: Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16), Cure Twist Female 8 Catheter (T8), Flexi-Seal AIR (with ENFit Connector)
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Convatec General & Plastic Surgery ✕
1 devices