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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K010975
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Product Description
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FDA Recall
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Varian Medical Systems Eclipse treatment planning system, Model Number H48, versions 6.5/7.x and In... 2 02/20/2009 Varian Medical Systems Oncology Systems
Varian Medical Systems Eclipse device, model H48, Version 6.5 is used to plan photon and electron ra... 2 09/17/2008 Varian Medical Systems Oncology Systems
Varian brand Radiation Therapy Linear Accelerator VARiS; VARiS Vision v6.5 up to and including v7... 2 01/18/2006 Varian Medical Systems Inc
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