Btg International, Inc. - FDA 510(k) Cleared Devices
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) cleared devices by Btg International, Inc.
6 devices
Cleared
Aug 23, 2019
EkoSonic Endovascular Device
Cardiovascular
119d
Cleared
Apr 05, 2019
EkoSonic Endovascular Device with Control Unit 4.0
Cardiovascular
122d
Cleared
Nov 26, 2018
EkoSonic Endovascular System
Cardiovascular
91d
Cleared
Mar 24, 2018
EKOS ultrasound EVD Device, EVD Control Unit
Neurology
262d
Cleared
Feb 24, 2017
EkoSonic Endovascular System with Control Unit 4.0
Cardiovascular
144d
Cleared
May 21, 2014
EKOSONIC MACH 4 ENDOVASCULAR DEVICE/EKOSONIC CONTROL UNIT
Cardiovascular
119d