ClearanceBrief
510(k) K033963 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

EP DEFLECTABLE CATHETERS

ApplicantEp Medsystems, Inc., West Berlin NJ, US
DecisionSubstantially Equivalent, Apr 15, 2004
ReceivedDec 22, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K033963

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.