Medical Device Recalls
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1 result found
510(K) Number: K984180 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Rubella IgM ELISA Test Kit. It is an enzyme-linked immunoabsorbent assay designed for the qualitati... | 3 | 07/30/2003 |
FEI # 2242436 Zeus Scientific Inc |
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