ClearanceBrief
510(k) K800400 ยท EBI Resin, Denture, Relining, Repairing, Rebasing

MAXUM DENTURE RESIN

ApplicantDentsply Intl., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 12, 1980
ReceivedFeb 26, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800400

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.