ArthroCare Corporation - FDA 510(k) Cleared Devices
Recent clearances: LYNX COBLATION Laryngeal Wand (72290254), FLOW 90? Wand, INTELLIO SHIFT System
36
Total
36
Cleared
0
Denied
FDA 510(k) Regulatory Record - ArthroCare Corporation Ear, Nose, Throat ✕
1 devices