Ikonos Corp. - FDA 510(k) Cleared Devices
Recent clearances: SEVRAIN CRANIAL CLAMP, SEVRAIN CRANIAL CLAMP (SCC-200 SERIES), TYMPANOSTOMY VENTILATION TUBE
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ikonos Corp. Ear, Nose, Throat ✕
1 devices