ClearanceBrief
510(k) K220556 ยท MUH System, X-Ray, Extraoral Source, Digital

OpenSensorX Series

ApplicantDentimax, Inc., Mesa AZ, US
DecisionSubstantially Equivalent, Apr 13, 2022
ReceivedFeb 28, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K220556

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.