Medical Device Recalls
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1 result found
510(K) Number: K232791 |
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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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| Access Intact PTH assay on the DxI 9000 Access Immunoassay Analyzer, Catalog number A16972, for the ... | 2 | 12/11/2024 | Beckman Coulter Inc. |
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