Neomed is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Neomed - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Neomed has 1 FDA 510(k) cleared medical devices. Based in Canada, N5v 3r6, GB.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Neomed Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neomed
1 devices