ClearanceBrief
510(k) K082642 ยท MUJ System, Planning, Radiation Therapy Treatment

ONCENTRA RT VIEWER 1.0

ApplicantNucletron Corporation, Columbia MD, US
DecisionSubstantially Equivalent, Nov 7, 2008
ReceivedSep 11, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082642

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.