ClearanceBrief
510(k) K833108 ยท DTB Permanent Pacemaker Electrode

BIOTRONIK I-UNIPOLAR PE-60/2-13

ApplicantBiotronik Sales, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 19, 1983
ReceivedSep 12, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833108

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.