Medical Device Recalls
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1 result found
510(K) Number: K113284 |
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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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FUJIFILM Digital Mammography System Aspire HD (FDR MS-1000) with Biopsy Positioner (FDR-1000BPY) ... | 2 | 08/30/2016 | Fujifilm Medical Systems U.S.A., Inc. |
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