ClearanceBrief
510(k) K160496 ยท NLH Catheter, Recording, Electrode, Reprocessed

Reprocessed Inquiry Steerable Diagnostic EP Catheter

ApplicantInnovative Health, LLC, Scottsdale AZ, US
DecisionSubstantially Equivalent, Jun 10, 2016
ReceivedFeb 22, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160496

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.