Medical Device Recalls
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1 result found
510(K) Number: K923506 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) UR3825 (2) UR3873 (3) UR8334 ... | 2 | 08/09/2023 | Randox Laboratories Ltd. |
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