ClearanceBrief
510(k) K972814 ยท DTB Permanent Pacemaker Electrode

LOCATOR MODEL 4036

ApplicantPacesetter, Inc., Sylmar CA, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Feb 23, 1998
ReceivedJul 29, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972814

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.