ClearanceBrief
510(k) K901789 ยท EBI Resin, Denture, Relining, Repairing, Rebasing

PALADON(R) 65

ApplicantKulzer, Inc., Chicago IL, US
DecisionSubstantially Equivalent, Jun 22, 1990
ReceivedApr 19, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901789

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.