Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K071681 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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. |
Cytomics FC 500 MPL Flow Cytometry System with MXP Software, Software Version 2.1, Automated differe... | 3 | 04/30/2008 | Beckman Coulter Inc |
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