Medical Device Recalls
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1 result found
510(K) Number: K171765 |
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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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| Adult Cap-ONE Biteblock REF YG-227T The cap-ONE Biteblock is intended to sample CO2 and administe... | 2 | 11/06/2024 |
FEI # 2080783 Nihon Kohden America Inc |
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