Medical Device Recalls
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1 result found
510(K) Number: K021819 |
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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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| LifeScan brand One Touch UltraSmart Meter Owners Booklet AW 060-788-01A; All One Touch UltraSmart... | 2 | 07/13/2005 |
FEI # 2939301 Lifescan Inc |
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