Medical Device Recalls
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1 result found
510(K) Number: K980386 |
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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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Gambro Prisma M100 preset, Part No. 8353486. | 2 | 04/05/2006 | Gambro Renal Products, Inc. |
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