ClearanceBrief
510(k) K203261 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

Reprocessed Inquiry Steerable Diagnostic EP Catheter

ApplicantInnovative Health, LLC, Scottsdale AZ, US
DecisionSubstantially Equivalent, Mar 5, 2021
ReceivedNov 5, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K203261

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.