Medical Device Recalls
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1 result found
510(K) Number: K220451 |
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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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Evidence MultiSTAT with software v 3.7-Analyzer intended for the qualitative determination of paren... | 3 | 05/09/2024 | Randox Laboratories Ltd. |
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