Mitsubishi Intl. Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Mitsubishi Intl. Corp. has 5 FDA 510(k) cleared medical devices. Based in Philadelphia, US.
Historical record: 5 cleared submissions from 1988 to 1996. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mitsubishi Intl. Corp. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Aug 06, 1996
MULTI LEAF COLLIMATOR
Radiology
131d
Cleared
Jan 17, 1996
EXL-12SP & 12DP LINAC
Radiology
245d
Cleared
Dec 21, 1995
EXL-15DP & 20-DP LINAC
Radiology
230d
Cleared
Aug 04, 1988
EXL-14 MEDICAL LINEAR ACCELERATOR
Radiology
206d
Cleared
Apr 29, 1988
EXL-22DP X-RAY RADIATION THERAPY SYSTEM
Radiology
249d