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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K071681
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Cytomics FC 500 MPL Flow Cytometry System with MXP Software, Software Version 2.1, Automated differe... 3 04/30/2008 Beckman Coulter Inc
1) Cytomics FC 500 With CXP Software BECKMAN COULTER 2) Cytomics FC 500 MPL With MXP Software BE... 1 11/20/2018 Beckman Coulter Inc.
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