Medical Device Recalls
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1 result found
510(K) Number: K032677 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| pocH-100i; sysmex; Automated Hematology Analyzer; 7.3" x 13.8" x 18.1" / 30.8 lbs.; Sysmex Corporati... | 2 | 10/18/2013 | Sysmex America Inc |
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