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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: K121328
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Agility. Version 3.0 of the Integrity interface and control software for the Elekta range of medica... 2 03/06/2014 FEI # 1037831
Elekta, Inc.
Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated for use when addition... 2 05/25/2013 FEI # 1037831
Elekta, Inc.
Multileaf Collimator To be used for single or multiple fractions, delivered as static and/or dyna... 2 09/10/2012 FEI # 1037831
Elekta, Inc.
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