Medical Device Recalls
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1 result found
510(K) Number: K122066 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Binding Site Optilite Beta-2-Microglobulin Urine Kit, Ref LK043.L.OPT.A, IVD. The firm name on the ... | 2 | 04/03/2018 |
FEI # 3002808340 The Binding Site Group, Ltd. |
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