Medical Device Recalls
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1 result found
510(K) Number: K141681 |
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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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Sysmex, Automated Hematology Analyzer XN Series, Sysmex Corporation, 1-5-1 Wakinohama-Kaigandori, Ch... | 2 | 04/14/2017 | Sysmex America Inc |
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