Cagent Vascular, LLC - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Cagent Vascular, LLC has 5 FDA 510(k) cleared medical devices. Based in Wayne, US.
Last cleared in 2022. Active since 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cagent Vascular, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Cagent Vascular, LLC
5 devices
Cleared
May 04, 2022
Serranator PTA Serration Balloon Catheter
Cardiovascular
55d
Cleared
Dec 15, 2021
Serranator PTA Serration Balloon Catheter
Cardiovascular
19d
Cleared
Dec 22, 2020
Serranator PTA Serration Balloon Catheter
Cardiovascular
29d
Cleared
Apr 15, 2020
Serranator PTA Serration Balloon Catheter
Cardiovascular
149d
Cleared
Feb 13, 2017
Serranator Alto PTA Serration Balloon Catheter
Cardiovascular
74d