Btg International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EkoSonic Endovascular Device, EkoSonic Endovascular Device with Control Unit 4.0, EkoSonic Endovascular System
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Btg International, Inc. Neurology ✕
1 devices