ClearanceBrief
510(k) K001414 ยท ELW Material, Impression

KWIKKMODEL

ApplicantR-Dental Dentalerzeugnisse GmbH, Hamburg, DE
DecisionSubstantially Equivalent, Aug 9, 2000
ReceivedMay 4, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001414

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.