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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: K091999
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FDA Recall
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CyberKnife Robotic Radiosurgery System with 4D Planning procedure option of MultiPlan Treatment Plan... 2 02/23/2012 FEI # 1000123585
Accuray Incorporated
CyberKnife Robotic Radiosurgery System: Lung Optimized Treatment option. The CyberKnife treatment... 2 01/11/2012 FEI # 1000123585
Accuray Incorporated
CyberKnife Robotic Radiosurgery System, medical charged-particle radiation therapy system, manufactu... 2 12/16/2010 FEI # 1000123585
Accuray Inc
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