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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K072079
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iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2 2 08/09/2019 Elekta, Inc.
IGuide System, software versions: 2.2.0, 2.2.1, 2.2.2 Product Usage: Linear Accelerator. The i... 2 07/25/2019 Medical Intelligence Medizintechnik Gmbh
HexaPOD evo RT System Product Usage: The intended use of the device is the control of accurate p... 2 08/30/2016 Elekta, Inc.
iGUIDE System, for patient positioning, with assistance of a 30 Tracking System in a radiotherapy en... 2 05/23/2016 Elekta, Inc.
iGUIDE System Product Usage: The intended use of the device is the control of accurate patient p... 2 06/17/2014 Elekta, Inc.
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