ClearanceBrief
510(k) K872231 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

BARD EPICARDIAL ELECTRODE ARRAY

ApplicantC.R. Bard, Inc., Billerica MA, US
DecisionSubstantially Equivalent, Oct 9, 1987
ReceivedJun 9, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K872231

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.