ClearanceBrief
510(k) K812830 ยท DTB Permanent Pacemaker Electrode

APC IMPLANTABLE PACING LEAD

ApplicantAmerican Pacemaker Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 18, 1982
ReceivedOct 8, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812830

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.