Medical Device Recalls
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1 result found
510(K) Number: K162411 |
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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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da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11 | 2 | 03/01/2022 | Intuitive Surgical, Inc. |
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