Viasonix , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Falcon/Xpress (Falcon/Xpress), Dolphin/IQ, Dolphin/4D and Dolphin/MAX with Dolphin/XF robot accessory, LiteWalk
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Viasonix , Ltd. Radiology ✕
4 devices