ClearanceBrief
510(k) K810582 ยท DTB Permanent Pacemaker Electrode

ELECTRODE, PACEMAKER PERMANENT

ApplicantPacesetter Systems, Mchenry IL, US
DecisionSubstantially Equivalent, Mar 13, 1981
ReceivedMar 3, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810582

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.