ClearanceBrief
510(k) K844349 ยท ELM Denture, Plastic, Teeth

SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS

ApplicantIvoclar USA, Inc., Chicago IL, US
DecisionSubstantially Equivalent, Dec 3, 1984
ReceivedNov 9, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844349

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.