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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K982713
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RT Desktop The EOS RT Desktop, as with the predicate SL/SLi Series user interface, is intended to... 2 03/06/2014 FEI # 1037831
Elekta, Inc.
Desktop Pro¿ R6.0 & R6.1, Linear Medical Accelerator. 3 02/07/2007 FEI # 1037831
Elekta, Inc.
Desktop Pro 4.2, 5.0, 5.1, 6.0, 6.2 A user interface of rthe SL/SLi Series Linear Accelerators th... 2 03/04/2011 FEI # 1037831
Elekta, Inc.
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