ClearanceBrief
510(k) K083591 ยท KPQ System, Simulation, Radiation Therapy

IKOENGELO, VERSION 2

ApplicantIkoetech, LLC, Houston TX, US
DecisionSubstantially Equivalent, Dec 29, 2008
ReceivedDec 4, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083591

No recall in the FDA data names this 510(k).

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