Medical Device Recalls
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1 result found
510(K) Number: K943812 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VIDAS Lyme IgG and IgM LYT, Ref #30 298, containing 60 LYT STR (reagent strip labels), 2 x 30 LYT S... | 2 | 07/20/2004 |
FEI # 1039284 Biomerieux, Inc. |
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