Medical Device Recalls
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1 result found
510(K) Number: K190999 |
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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 Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip RE... | 2 | 04/22/2022 | Intuitive Surgical, Inc. |
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