ClearanceBrief
510(k) K903672 ยท EKO Denture Preformed (Partially Prefabricated Denture)

DENE BRIDGE

ApplicantDirotian Pty. , Ltd., South Australia, AU
DecisionSubstantially Equivalent, Dec 5, 1990
ReceivedAug 14, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903672

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.