Medical Device Recalls
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1 result found
510(K) Number: K140189 |
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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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| EndoWrist One Vessel Sealer, 8MM, IS4000, 6 pack used in conjunction with the da Vinci Surgical Sys... | 2 | 02/24/2015 | Intuitive Surgical, Inc. |
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