ClearanceBrief
510(k) K870610 ยท DTB Permanent Pacemaker Electrode

RESUBMISSION OF MODEL 030-437 IMPLANT. ELECTRODE

ApplicantTelectronics, Inc., Suffield CT, US
DecisionSubstantially Equivalent, Mar 20, 1987
ReceivedFeb 2, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870610

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.