Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K093954 |
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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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BioPlex 2200, Anti-CCP Calibrator Set, REF 663-3200, IVD | 2 | 04/12/2023 | Bio-Rad Laboratories, Inc. |
BioPlex 2200, Anti-CCP Reagent Pack, REF 665-3250, IVD | 2 | 04/12/2023 | Bio-Rad Laboratories, Inc. |
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