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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
510(K) Number: K092132
 
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Product Description
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FDA Recall
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XiO Radiation Treatment Planning System, XiO Release 2.1.0 and above Used to create treatment pla... 2 06/20/2011 Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, XiO Release 4.0.2 and above Used to create treatment plans... 2 06/20/2011 Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, XiO Release 4.50.00 and above 2 06/20/2011 Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, XiO Release 4.0.0 through 4.40.00 Used to create treatme... 2 06/16/2011 Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, XiO Release 4.3.0 and above Used to create treatment pla... 2 06/16/2011 Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, XiO Release 1.5.0 and above. Used to create treatment pl... 2 06/15/2011 Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, XiO Release 4.3.0 through 4.50.00. Used to create treatm... 2 06/15/2011 Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, XiO Release 4.3.1 through 4.40.00. Used to create treat... 2 06/15/2011 Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, XiO Release 1.0.2 and above. Used to create treatment pl... 2 06/03/2011 Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, XiO Release 4.50.00 and above Used to create treatment p... 2 06/02/2011 Computerized Medical Systems Inc
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