Medel S.P.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medel S.P.A. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Medel S.P.A. has 4 FDA 510(k) cleared medical devices. Based in Cary, US.
Historical record: 4 cleared submissions from 2006 to 2009. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Medel S.P.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medel S.P.A.
4 devices