Ion Beam Application S.A. is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Ion Beam Application S.A. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ion Beam Application S.A. has 1 FDA 510(k) cleared medical devices. Based in Louvain-La-Neuve, BE.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ion Beam Application S.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ion Beam Application S.A.
1 devices