Neurozone Msh Incorporated is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Neurozone Msh Incorporated - FDA 510(k) Cleared Devices
Recent clearances: Esprit Nova
1
Total
1
Cleared
0
Denied
Neurozone Msh Incorporated has 1 FDA 510(k) cleared medical devices. Based in Dundas, CA.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neurozone Msh Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neurozone Msh Incorporated
1 devices