Medical Device Recalls
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1 result found
510(K) Number: K953896 |
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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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Delphi IVantage Volumetric Ambulatory Infusion Pump/System; Ref nos. 12864051FRE, Rev. 8 and 1286405... | 2 | 08/26/2006 | Delphi Medical Systems |
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