ClearanceBrief
510(k) K895742 ยท EBI Resin, Denture, Relining, Repairing, Rebasing

LITELINE VLC SOFT RELINE

ApplicantDentsply Intl., York PA, US
DecisionSubstantially Equivalent, Dec 18, 1989
ReceivedSep 26, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895742

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.