ClearanceBrief
510(k) K905831 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

ARZCO OCTAPOLAR ESOPHAGEAL CARDIAC RECORD CATH

ApplicantArzco Medical Electronics, Inc., Vernon Hills IL, US
DecisionSubstantially Equivalent, Mar 29, 1991
ReceivedDec 31, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905831

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.