Medical Device Recalls
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1 result found
510(K) Number: K021988 |
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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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| Continuum MR Compatible Infusion Pump. Pump Model #3009135 | 2 | 05/13/2005 |
FEI # 2520313 Medrad Inc |
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