ClearanceBrief
510(k) K864618 ยท DTB Permanent Pacemaker Electrode

IMPLANTABLE ELECTRODE LEAD, MODEL 030-439

ApplicantTelectronics, Inc., Suffield CT, US
DecisionSubstantially Equivalent, May 21, 1987
ReceivedNov 24, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864618

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.