Medical Device Manufacturer · US , Bothell , WA

Btg International, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2014

Recent clearances: EkoSonic Endovascular Device, EkoSonic Endovascular Device with Control Unit 4.0, EkoSonic Endovascular System

6
Total
6
Cleared
0
Denied

Btg International, Inc. has 6 FDA 510(k) cleared medical devices. Based in Bothell, US.

Historical record: 6 cleared submissions from 2014 to 2019. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Btg International, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Btg International, Inc.

6 devices
1-6 of 6
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