ClearanceBrief
510(k) K863582 ยท DXY Implantable Pacemaker Pulse-Generator

MODEL 725TH HANDHELD TRANSCEIVER (PROGRAMMER)

ApplicantCook Pacemaker Corp., Leechburg PA, US
DecisionSubstantially Equivalent, Oct 8, 1986
ReceivedSep 15, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863582

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.