Medical Device Recalls
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1 result found
510(K) Number: K023471 |
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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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| Disetronic H-TRONplus Insulin Pump; catalog # 8050023 [clear case], 8050064 [blue case], 8050021 [so... | 2 | 09/17/2003 | Roche Diagnostics Corp. |
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