A.B.M. Italia S.P.A is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
A.B.M. Italia S.P.A - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
A.B.M. Italia S.P.A has 1 FDA 510(k) cleared medical devices. Based in Roncadelle Di Ormelle, IT.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by A.B.M. Italia S.P.A Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - A.B.M. Italia S.P.A
1 devices