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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K102216
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Product Description
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FDA Recall
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XiO Radiation Treatment Planning System. XiO Release 4.50.00 and above Used to create treatment p... 2 06/17/2011 FEI # 1937649
Computerized Medical Systems Inc
XiO Radiation Treatment Planning System. Used to create treatment plans for any cancer patient for ... 2 10/16/2015 FEI # 1037831
Elekta, Inc.
XiO Radiation Treatment Planning System, XiO versions equal to or greater than 2.4.0 and less than 4... 2 08/03/2011 FEI # 1937649
Computerized Medical Systems Inc
XiO Radiation Treatment Planning System, Versions 4.30.00-4.64.00. Used to create treatment plans... 2 05/22/2012 FEI # 1937649
Computerized Medical Systems Inc
XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radi... 2 02/04/2014 FEI # 1037831
Elekta, Inc.
XiO RTP System The XiO RTP System is used to create treatment plans for any cancer patient for wh... 2 01/17/2014 FEI # 1037831
Elekta, Inc.
XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for wh... 2 03/13/2014 FEI # 1037831
Elekta, Inc.
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