Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K001574 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of IgG and... | 3 | 08/23/2018 | Euro Diagnostica AB |
| is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of IgG and... | 3 | 08/23/2018 | Euro Diagnostica AB |
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