ClearanceBrief
Company ยท CA

Mds Nordion

FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2006. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MOTIrradiator, Blood To Prevent Graft Versus Host Disease3
MUJSystem, Planning, Radiation Therapy Treatment3
IWBSystem, Radiation Therapy, Radionuclide2
JAICouch, Radiation Therapy, Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 15, 2006K060870AVANZA
Mds Nordion, CA
JAI
Mar 9, 2006K053485THERATRON EQUINOX, MODELS 80 CM AND 100 CM
Mds Nordion, Inc., CA
IWB
May 26, 2005K051065RAYCELL X-RAY BLOOD IRRADIATOR
Mds Nordion, CA
MOT
May 20, 2005K050963GAMMACELL 1000 ELITE AND GAMMACELL 3000 ELAN
Mds Nordion, CA
MOT
Sep 26, 2003K032684RAYCELL
Mds Nordion, CA
MOT
Jun 6, 2002K020971DCM 2.0
Mds Nordion AB, CA
MUJ
Jun 5, 2001K010682HELAX-TMS V 5.1 RADIATION THERAPY TREATMENT PLANNING SYSTEM
Mds Nordion, CA
MUJ
May 23, 2001K011246DCM 1.0
Mds Nordion, CA
MUJ
Apr 27, 2000K001006THERATRON 780C/1000 WITH COMPUTERIZED CONSOLE UPGRADE
Mds Nordion, CA
IWB

Latest recalls

DateFirm and productCodeLinked 510(k)
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