Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K141077 |
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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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Fluorescence Imaging Procedure Kits used with the da Vinci Si and Xi Surgical Systems; Model number... | 2 | 09/17/2015 | Intuitive Surgical, Inc. |
Fluorescence Imaging Procedure Kit, designed for use with Firefly Fluorescence Imaging for the da V... | 2 | 12/19/2014 | Intuitive Surgical, Inc. |
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