ClearanceBrief
510(k) K213477 ยท EKZ Unit, Electrosurgical, And Accessories, Dental

Root ZX3

ApplicantJ. Morita USA, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Aug 3, 2022
ReceivedOct 29, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K213477

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.