ClearanceBrief
510(k) K211317 ยท MUH System, X-Ray, Extraoral Source, Digital

CRUXVIEW

ApplicantCruxell Corp., Daejeon, KR
DecisionSubstantially Equivalent, Jul 29, 2021
ReceivedApr 30, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K211317

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.