ClearanceBrief
510(k) K823892 ยท DTB Permanent Pacemaker Electrode

MODEL SZ PACEMAKER LEAD-VARIOUS

ApplicantDr. Ing. P. Osypka, GmbH, Mchenry IL, US
DecisionSubstantially Equivalent, Apr 30, 1983
ReceivedDec 27, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823892

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.