ClearanceBrief
510(k) K810491 ยท DTB Permanent Pacemaker Electrode

TYPE YC ENDOCARDIAL LEAD

ApplicantBiotronik Sales, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 20, 1981
ReceivedFeb 24, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810491

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.