ClearanceBrief
510(k) K792604 ยท DTB Permanent Pacemaker Electrode

LIFELINE TLE ENDOCARDIAL PACING LEAD,

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 31, 1979
ReceivedDec 18, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792604

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.