Medical Device Recalls
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1 result found
510(K) Number: K891081 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Cytomegalovirus (CMV) IgG ELISA Test System, In-Vitro Diagnostic, manufactured by Zeus Scientific, I... | 2 | 08/12/2003 | Zeus Scientific Inc |
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