Medical Device Recalls
-
1 to 7 of 7 Results
510(K) Number: K072504 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
CyberKnife System Robotic Radiosurgery System, (Standard Treatment Couch) Synchrony Respiratory Trac... | 2 | 01/18/2011 | Accuray Inc |
CyberKnife System Robotic Radiosurgery System, (Robocouch Patient positioning System) Synchrony Resp... | 2 | 01/18/2011 | Accuray Inc |
RoboCouch Patient Support System, model number 025007, a subsystem of the Cyberknife Robotic Radiosu... | 2 | 01/11/2011 | Accuray Inc |
CyberKnife Treatment Delivery System, a subsystem of the CyberKnife Robotic Radiosurgery System, man... | 2 | 09/14/2009 | Accuray Inc |
Cyberknife Robotic Radiosurgery System. A radiation therapy device, MultiPlan (MP) Treatment Planni... | 2 | 01/17/2009 | Accuray Inc |
CyberKnife Robotic Radiosurgery System radiation therapy device with Multiplan treatment Planning So... | 2 | 09/17/2008 | Accuray Inc |
Accuracy Cyberknife Robotic Radiosurgery System, medical charged particle radiation therapy device. ... | 2 | 09/16/2008 | Accuray Inc |
-