Medical Device Recalls
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1 result found
510(K) Number: K150879 |
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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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| LIAISON 1-84 PTH Assay - Product Usage: is an in vitro chemiluminescent immunoassay (CLIA) intended ... | 2 | 04/01/2021 | Diasorin Inc. |
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