ClearanceBrief
510(k) K802295 ยท DTB Permanent Pacemaker Electrode

POLY FLEX IMPLANTABLE PACING LEAD

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 9, 1981
ReceivedSep 19, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802295

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.