ClearanceBrief
510(k) K240826 · NLH Catheter, Recording, Electrode, Reprocessed

Reprocessed DECANAV™ Electrophysiology Catheter; Reprocessed WEBSTER® Duo-Decapolar Electrophysiology Catheter

ApplicantSterilmed, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Oct 11, 2024
ReceivedMar 26, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240826

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.