Medical Device Recalls
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1 result found
510(K) Number: K944426 |
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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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| Osom Ultra hCG Combo Test- IVD immunoassay for the qualitative detection of human chorionic gonadotr... | 2 | 10/30/2024 | Princeton Biomeditech Corp |
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