ClearanceBrief
510(k) K780722 ยท EKO Denture Preformed (Partially Prefabricated Denture)

ADVANCED DENTURE SYSTEM

ApplicantAdvanced Marketing Research Co., Mchenry IL, US
DecisionSubstantially Equivalent, May 26, 1978
ReceivedMay 1, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780722

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.