Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K191280 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with ... | 2 | 08/01/2022 | Intuitive Surgical, Inc. |
DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi', Single Use Instrument 8mm, REF 480440 | 2 | 05/31/2022 | Intuitive Surgical, Inc. |
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