Medical Device Recalls
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1 result found
510(K) Number: K082988 |
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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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Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated Endos... | 2 | 12/22/2023 | Steris Corporation |
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