Mds Nordion - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Mds Nordion has 7 FDA 510(k) cleared medical devices. Based in Ottawa, CA.
Historical record: 7 cleared submissions from 2000 to 2006. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mds Nordion Filter by specialty or product code using the sidebar.
7 devices
Cleared
May 15, 2006
AVANZA
Radiology
46d
Cleared
May 26, 2005
RAYCELL X-RAY BLOOD IRRADIATOR
Radiology
30d
Cleared
May 20, 2005
GAMMACELL 1000 ELITE AND GAMMACELL 3000 ELAN
Radiology
32d
Cleared
Sep 26, 2003
RAYCELL
Radiology
28d
Cleared
Jun 05, 2001
HELAX-TMS V 5.1 RADIATION THERAPY TREATMENT PLANNING SYSTEM
Radiology
90d
Cleared
May 23, 2001
DCM 1.0
Radiology
30d
Cleared
Apr 27, 2000
THERATRON 780C/1000 WITH COMPUTERIZED CONSOLE UPGRADE
Radiology
29d