Ion Beam Applications S.A. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Ion Beam Applications S.A. has 13 FDA 510(k) cleared radiology devices. Based in Philadelphia, US.
Historical record: 13 cleared submissions from 2001 to 2017.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
13 devices
Cleared
Aug 17, 2017
IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus...
Radiology
247d
Cleared
Jul 10, 2014
GANTRY BEAM LINE
Radiology
296d
Cleared
Nov 20, 2013
I2C
Radiology
70d
Cleared
Aug 06, 2010
MODIFICATION TO IBA PROTON THERAPY SYSTEM-PROTEUS 235
Radiology
66d
Cleared
Jul 21, 2010
IBA PROTON THERAPY SYSTEM, MODEL PROTEUS 235
Radiology
126d
Cleared
Dec 22, 2009
IBA PROTON THERAPY SYSTEM, PROTEUS 235
Radiology
102d
Cleared
Aug 11, 2009
PROTEUS 235 PROTON THERAPY SYSTEM
Radiology
69d
Cleared
Apr 15, 2009
IBA PROTON THERAPY SYSTEM - PROTEUS 235
Radiology
183d
Cleared
Dec 12, 2008
IBA PROTON THERAPY SYSTEM- PROTEUS 235
Radiology
113d
Cleared
Jul 28, 2006
IBA PROTON THERAPY SYSTEM - PROTEUS 235
Radiology
22d
Cleared
Apr 11, 2006
IBA PROTON THERAPY SYSTEM - PROTEUS 235
Radiology
26d
Cleared
Jan 24, 2006
IBA PROTON THERAPY SYSTEM-PROTEUS 235
Radiology
25d
Cleared
Jul 12, 2001
PROTON THERAPY SYSTEM
Radiology
1046d