Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K182371 |
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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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Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098 | 2 | 04/11/2024 | Intuitive Surgical, Inc. |
da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/... | 2 | 12/27/2021 | Intuitive Surgical, Inc. |
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