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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K063220
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Product Description
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Recall
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FDA Recall
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da Vinci S. Surgical System, da Vinci Si and da Vinci Si-e Surgical Systems. Intuitive Surgical, ... 2 03/13/2012 Intuitive Surgical, Inc.
Intuitive brand da Vinci S Surgical System, Endoscopic Instrument Control System, Model IS1200 with ... 2 02/22/2008 Intuitive Surgical, Inc.
Intuitive brand da Vinci S Surgical System, Endoscopic Instrument Control System, Model IS2000 with ... 2 02/22/2008 Intuitive Surgical, Inc.
daVinci S Surgical system, patient side cart Auxiliary power board (APB) (printed circuit board asse... 2 09/26/2007 Intuitive Surgical, Inc.
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