ClearanceBrief
510(k) K062251 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

REFLEXION SPIRAL VARIABLE RADIUS CATHETER, MODEL 402804

ApplicantSt Jude Medical, Minnetonka MN, US
DecisionSubstantially Equivalent, Oct 20, 2006
ReceivedAug 3, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062251

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.