ClearanceBrief
510(k) K160421 ยท NLH Catheter, Recording, Electrode, Reprocessed

Reprocessed Inquiry Optima Plus Steerable Diagnostic EP Catheter, Reprocessed Inquiry Optima Steerable Diagnostic EP Catheter

ApplicantInnovative Health, LLC, Scottsdale AZ, US
DecisionSubstantially Equivalent, Nov 2, 2016
ReceivedFeb 16, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160421

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.