ClearanceBrief
510(k) K933451 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

OPEN TIP MULTI-ELECTRODE CATHETER, MODIFICATION

ApplicantElectro-Catheter Corp., Rahway NJ, US
DecisionSubstantially Equivalent, Apr 19, 1995
ReceivedJul 12, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933451

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.