Medical Device Recalls
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1 result found
510(K) Number: K981021 |
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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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| Cardiolipin IgM ELISA Test System, Product Number 438450CE. The test kit consists of a test plate, ... | 3 | 11/20/2004 |
FEI # 2242436 Zeus Scientific Inc |
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