Cerus Endovascular, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Cerus Endovascular, Inc. has 2 FDA 510(k) cleared medical devices. Based in Fremont, US.
Last cleared in 2022. Active since 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cerus Endovascular, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Cerus Endovascular, Inc.
2 devices