ClearanceBrief
510(k) K933417 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

ECHOMARK(R) ELECTROPHYSIOLOGY CATHETER

ApplicantEchocath, Inc., Princeton NJ, US
DecisionSubstantially Equivalent, May 4, 1995
ReceivedJul 13, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933417

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.