Emovi is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Emovi - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Emovi has 1 FDA 510(k) cleared medical devices. Based in Montreal, Quebec, CA.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Emovi Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Emovi
1 devices