ClearanceBrief
510(k) K802293 ยท DTB Permanent Pacemaker Electrode

POLYFLEX IMPLANTABLE PACING LEAD

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 31, 1980
ReceivedSep 19, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802293

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.