ClearanceBrief
510(k) K930069 ยท LDF Electrode, Pacemaker, Temporary

BIPOLAR BALLOON PACING CATHETER BY J-LLOYD

ApplicantJ-Lloyd Medical, Inc., West Berlin NJ, US
DecisionSubstantially Equivalent, Jan 28, 1994
ReceivedJan 6, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930069

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.