Headsense Medical, Inc. is one of 5577 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Headsense Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Neuro Assessment System NAS-1000
1
Total
1
Cleared
0
Denied
Headsense Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Akron, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Headsense Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Headsense Medical, Inc.
1 devices