ClearanceBrief
510(k) K020294 ยท IYE Accelerator, Linear, Medical

MOTION TRACKING

ApplicantAccuray, Inc., Sunnyvale CA, US
DecisionSubstantially Equivalent, Apr 22, 2002
ReceivedJan 28, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020294

DateFirm and productCodeLinked 510(k)
Jan 18, 2011Accuray Inc
CyberKnife System Robotic Radiosurgery System, (Standard Treatment Couch) Synchrony Respiratory Tracking System, a Radiation Therapy Device, Model Numbers: 026429, 028185, Product is manufactured and
Terminated
IYENone listed
Jan 18, 2011Accuray Inc
CyberKnife System Robotic Radiosurgery System, (Robocouch Patient positioning System) Synchrony Respiratory Tracking System, a Radiation therapy device, Model Numbers: 026430, 028186, Product is manuf
Terminated
IYENone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.