Medical Device Recalls
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1 result found
510(K) Number: K993064 |
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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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| Prisma continuous renal replacement system. | 1 | 10/01/2005 |
FEI # 1713683 Gambro Renal Products |
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