M.V.S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
M.V.S.R.L. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
M.V.S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Abano Terme, IT.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by M.V.S.R.L. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - M.V.S.R.L.
1 devices