Medical Device Recalls
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1 result found
510(K) Number: K191635 |
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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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OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565 | 2 | 02/19/2020 | The Binding Site Group, Ltd. |
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