ClearanceBrief
510(k) K810286 ยท DTB Permanent Pacemaker Electrode

PACEPATH IMPLANT. ENDOCARD. PACING LEAD

ApplicantPacesetter Systems, Mchenry IL, US
DecisionSubstantially Equivalent, Nov 27, 1981
ReceivedFeb 2, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810286

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.