ClearanceBrief
510(k) K233825 ยท NLH Catheter, Recording, Electrode, Reprocessed

Reprocessed Webster Duo-Decapolar Diagnostic EP Catheter

ApplicantInnovative Health, Scottsdale AZ, US
DecisionSubstantially Equivalent, Jun 7, 2024
ReceivedDec 1, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233825

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.