Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K090993 |
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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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Thyroidectomy Indication for the da Vinci Surgical Systems; Product Usage: da Vinci Thyroidectom... | 2 | 05/29/2013 | Intuitive Surgical, Inc. |
User Manual addendum, TORS for da Vinci Surgical System IS 1200, IS 2000 and IS 3000. Product Us... | 2 | 05/29/2013 | Intuitive Surgical, Inc. |
Intuitive Surgical da Vinci Si Surgical System (IS3000); Mfg by: Intuitive Surgical, Sunnyvale, CA ... | 2 | 08/03/2011 | Intuitive Surgical, Inc. |
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