Medical Device Recalls
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1 result found
510(K) Number: K013309 |
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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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| Amigo Insulin Infusion Pump | 2 | 09/14/2004 |
FEI # 3003352163 Nipro Diabetes Systems, Inc. |
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