ClearanceBrief
510(k) K171277 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

Reprocessed Inquiry Steerable Diagnostic EP Catheter

ApplicantInnovative Health, LLC, Scottsdale AZ, US
DecisionSubstantially Equivalent, Oct 23, 2017
ReceivedMay 1, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171277

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.