ClearanceBrief
510(k) K963074 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

HARMAC QUADPOLAR MAPPING PACING CATHETER

ApplicantHarmac Medical Products, Inc., Buffalo NY, US
DecisionSubstantially Equivalent, Jun 25, 1997
ReceivedJun 28, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963074

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.