Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K041478 |
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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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| BD Logic -- Blood Glucose Monitor. | 2 | 02/25/2006 |
FEI # 2243072 Becton Dickinson & Company |
| Paradigm Link -- Blood Glucose Monitor. | 2 | 02/25/2006 |
FEI # 2243072 Becton Dickinson & Company |
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