Medical Device Recalls
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1 result found
510(K) Number: K946090 |
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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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| VITROS XT Chemistry Products ALKP Slides | 2 | 09/21/2023 |
FEI # 1000305840 Ortho-Clinical Diagnostics, INc. |
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