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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 34 of 34 Results
510(K) Number: K050369
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Product Description
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FDA Recall
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da Vinci S Surgical System, Model number IS2000 Endoscopic Instrument Control System, manufactured b... 2 09/16/2008 FEI # 3001675293
Intuitive Surgical, Inc.
da Vinci S Surgical System, Model number IS2000 Revision number A51 P5; endoscopic surgical control ... 2 06/12/2008 FEI # 3001675293
Intuitive Surgical, Inc.
da Vinci Si Surgeon Console. Intended to assist in the accurate Control of Intuitive Surgical End... 2 05/29/2013 FEI # 3001675293
Intuitive Surgical, Inc.
daVinci S Surgical system, patient side cart Auxiliary power board (APB) (printed circuit board asse... 2 09/26/2007 FEI # 3001675293
Intuitive Surgical, Inc.
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