ClearanceBrief
510(k) K190127 ยท NLH Catheter, Recording, Electrode, Reprocessed

Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheter

ApplicantInnovative Health, LLC, Scottsdale AZ, US
DecisionSubstantially Equivalent, Aug 23, 2019
ReceivedJan 28, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190127

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.