Vmi Technologies is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Vmi Technologies - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Vmi Technologies has 1 FDA 510(k) cleared medical devices. Based in Ottawa,Ontario, CA.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Vmi Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vmi Technologies
1 devices