Medical Device Recalls
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1 result found
510(K) Number: K993208 |
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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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| Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination of methamphetamine in o... | 3 | 03/05/2021 |
FEI # 3004142665 OraSure Technologies, Inc. |
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