Medical Device Recalls
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1 result found
510(K) Number: K071967 |
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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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| Sysmex XE-5000 Automated Hematology System; an automated differential cell counter; Sysmex Corporat... | 2 | 11/06/2012 |
FEI # 1000515253 Sysmex America, Inc. |
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