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.
510(k) submissions have been managed by Cerus Endovascular, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Cerus Endovascular, Inc.
2 devices