Medical Device Recalls
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1 result found
510(K) Number: K200533 |
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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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binx io CT/NG Assay- Single-use Cartridge for the qualitative detection of Chlamydia trachomatis and... | 2 | 05/23/2023 | Binx Health, Inc. |
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