Medical Device Recalls
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1 result found
510(K) Number: K922992 |
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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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| Terumo Custom Cardioplegia Delivery Set- Catalog Number:165720 and Catalog Number: 6375 Product ... | 2 | 10/31/2014 |
FEI # 1000149028 Terumo Cardiovascular Systems Corp |
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