Medical Device Recalls
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1 result found
510(K) Number: K092387 |
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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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| Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface b... | 2 | 08/08/2024 | Steris Corporation |
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