Cerebra Medical , Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Cerebra Medical , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Cerebra Sleep System
1
Total
1
Cleared
0
Denied
Cerebra Medical , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Winnipeg, CA.
Last cleared in 2022. Active since 2022. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cerebra Medical , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cerebra Medical , Ltd.
1 devices