Medical Device Recalls
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1 result found
510(K) Number: K012521 |
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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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| BinaxNOW Respiratory Strep A Test Kit, CLIA Waived, Catalog Number 730025 | 2 | 09/19/2024 |
FEI # 1451040 Cypress Medical Products LLC |
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