ClearanceBrief
510(k) K911065 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

ARROW QUADPOLAR MAPPING/PACING CATHETER

ApplicantArrow Intl., Inc., Reading PA, US
DecisionSubstantially Equivalent, Jun 18, 1992
ReceivedMar 13, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911065

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.