ClearanceBrief
510(k) K010800 ยท EBI Resin, Denture, Relining, Repairing, Rebasing

VERSYO.COM

ApplicantHeraeus Kulzer, Inc., Armonk NY, US
DecisionSubstantially Equivalent, May 31, 2001
ReceivedMar 16, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010800

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.