ClearanceBrief
510(k) K902115 ยท EBI Resin, Denture, Relining, Repairing, Rebasing

PALAPRESS(R) VARIO RESIN

ApplicantKulzer, Inc., Chicago IL, US
DecisionSubstantially Equivalent, Jul 27, 1990
ReceivedMay 10, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902115

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.