ClearanceBrief
510(k) K022741 ยท MUJ System, Planning, Radiation Therapy Treatment

SPOT PRO (220V), MODEL 131.099

ApplicantNucletron Corporation, Columbia MD, US
DecisionSubstantially Equivalent, Oct 24, 2002
ReceivedAug 19, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K022741

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.