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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K042146
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Product Description
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FDA Recall
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RoboCouch Patient Positioning System Product Usage: is intended for use in the support and pos... 2 04/20/2013 FEI # 1000123585
Accuray Incorporated
RoboCouch Patient Support System, a component of the CyberKnife Robotic Radiosurgery System. Model n... 2 01/14/2009 FEI # 1000123585
Accuray Inc
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