ClearanceBrief
510(k) K901037 ยท EKS File, Pulp Canal, Endodontic

VISIONER 21-A

ApplicantJ. Morita USA, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Aug 14, 1990
ReceivedMar 6, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901037

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.