Medical Device Recalls
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1 result found
510(K) Number: K911385 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Coulter MAXM Hematology Analyzer and MAXM Hematology Analyzer with Autoloader. Hematology Analyze... | 2 | 03/18/2011 | Beckman Coulter Inc. |
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