ClearanceBrief
510(k) K812032 ยท IYE Accelerator, Linear, Medical

MEVATRON 67E

ApplicantSiemens Medical Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 18, 1981
ReceivedJul 20, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812032

DateFirm and productCodeLinked 510(k)
Jan 25, 2017Siemens Medical Solutions USA, Inc
MEVATRON M 6730/6740 (MEX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of c
Terminated
IYENone listed

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