Ion Beam Application S.A. is one of 47 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
Recent clearances: Proton Therapy System - Proteus 235 (Proteus One, Proteus Plus, Proteus TK2)
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.
510(k) submissions have been managed by Saul Ewing Llp as regulatory consultant.
FDA 510(k) Regulatory Record - Ion Beam Application S.A.
1 devices