Insightec , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Exablate Model 2100V1, Exablate Prostate System, Exablate MRgFUS, Exablate 2100V1 Type 3.0
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Insightec , Ltd. Gastroenterology & Urology ✕
1 devices