Medical Device Recalls
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1 result found
510(K) Number: K151465 |
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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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| CS-7, Model No. A4C1 | 2 | 06/22/2018 |
FEI # 2241281 Konica Minolta Medical Imaging USA, Inc. |
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