Ensite Vascular - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ensite Vascular has 2 FDA 510(k) cleared medical devices. Based in Olathe, US.
Last cleared in 2021. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ensite Vascular Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Brosseau Consulting, LLC as regulatory consultant.
2 devices