Medical Device Recalls
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1 result found
510(K) Number: K984527 |
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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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LifeScan OneTouch Data Management Software Version 1.0, Part Number: 021-722-01(for OneTouch Select ... | 3 | 04/08/2008 | Lifescan Inc |
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