ClearanceBrief
510(k) K874205 ยท DTB Permanent Pacemaker Electrode

ENDOCARDIAL SCREW-IN LEAD, MODEL 1018T

ApplicantPacesetter Systems, Sylmar CA, US
DecisionSubstantially Equivalent, Feb 2, 1988
ReceivedOct 15, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874205

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.