ClearanceBrief
510(k) K182488 ยท NLH Catheter, Recording, Electrode, Reprocessed

Reprocessed Response Diagnostic Electrophysiology Catheter

ApplicantInnovative Health, LLC, Scottsdale AZ, US
DecisionSubstantially Equivalent, Feb 22, 2019
ReceivedSep 11, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182488

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.