ClearanceBrief
510(k) K231202 ยท MUH System, X-Ray, Extraoral Source, Digital

QuickRayPRO

ApplicantDenterprise International, Inc., Ormond Beach FL, US
DecisionSubstantially Equivalent, Jun 22, 2023
ReceivedApr 27, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231202

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.