Neuroservo, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Neuroservo, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VEEGix EEG System
1
Total
1
Cleared
0
Denied
Neuroservo, Inc. has 1 FDA 510(k) cleared medical devices. Based in Montreal, CA.
Latest FDA clearance: Aug 2024. Active since 2024. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuroservo, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neuroservo, Inc.
1 devices