Cerebrotech Medical Systems is one of 20656 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cerebrotech Medical Systems - FDA 510(k) Cleared Devices
Recent clearances: Cerebrotech CMS-5000
1
Total
1
Cleared
0
Denied
Cerebrotech Medical Systems has 1 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cerebrotech Medical Systems Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pamela M. Buckman, Msn as regulatory consultant.
FDA 510(k) Regulatory Record - Cerebrotech Medical Systems
1 devices