ClearanceBrief
510(k) K792536 ยท DTE Pulse-Generator, Pacemaker, External

CYNERGY MODEL 182

ApplicantCynergy, Mchenry IL, US
DecisionSubstantially Equivalent, Jan 31, 1980
ReceivedDec 7, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792536

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.