ClearanceBrief
510(k) K140013 ยท MUH System, X-Ray, Extraoral Source, Digital

SOPIX INSIDE, SOPIX2 INSIDE

ApplicantSopro - Acteon Group, Mt Laurel NJ, US
DecisionSubstantially Equivalent, Sep 5, 2014
ReceivedJan 2, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140013

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.