Medical Device Recalls
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1 result found
510(K) Number: K220023 |
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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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| 8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179 | 2 | 01/10/2025 | Intuitive Surgical, Inc. |
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