ClearanceBrief
510(k) K810398 ยท DTB Permanent Pacemaker Electrode

APC IMPLANTABLE PACING LEAD, MODEL 3266

ApplicantAmerican Pacemaker Corp., Mchenry IL, US
DecisionSubstantially Equivalent, May 15, 1981
ReceivedFeb 18, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810398

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.