ClearanceBrief
510(k) K810538 ยท EAG Cephalometer

PLASTICEPH

ApplicantMorningstar Dental Co., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 29, 1981
ReceivedFeb 26, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810538

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.