Mds Nordion AB

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K060870AVANZAMay 15, 2006
K053485THERATRON EQUINOX, MODELS 80 CM AND 100 CMMarch 9, 2006
K051065RAYCELL X-RAY BLOOD IRRADIATORMay 26, 2005
K050963GAMMACELL 1000 ELITE AND GAMMACELL 3000 ELANMay 20, 2005
K032684RAYCELLSeptember 26, 2003
K020971DCM 2.0June 6, 2002
K010682HELAX-TMS V 5.1 RADIATION THERAPY TREATMENT PLANNING SYSTEMJune 5, 2001
K011246DCM 1.0May 23, 2001
K001006THERATRON 780C/1000 WITH COMPUTERIZED CONSOLE UPGRADEApril 27, 2000