ClearanceBrief
510(k) K810643 ยท LDF Electrode, Pacemaker, Temporary

UNIVERSAL PACING ELECTRODE KIT

ApplicantStanco Medical, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 8, 1981
ReceivedMar 10, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810643

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.