Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K122137 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CyberKnife Robotic Radiosurgery System using software version 10.6; Catalog/Part Number: 54000 UDI... | 2 | 12/12/2016 | Accuray Incorporated |
CyberKnife Robotic Radiosurgery System with the first generation IRIS Variable Aperture Collimator. ... | 2 | 11/14/2014 | Accuray Incorporated |
Accuray CyberKnife Robotic Radiosurgery System; Accuray Incorporated Sunnyvale, CA. Indicated for... | 2 | 01/27/2014 | Accuray Incorporated |
Accuray CyberKnife System Medical Physicist, Robotic Radiosurgery System, Medical charged-particle r... | 2 | 04/16/2013 | Accuray Incorporated |
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