ClearanceBrief
510(k) K811066 ยท DXY Implantable Pacemaker Pulse-Generator

MODEL 230-06 CYBERLITH TM I BIPOLAR IN

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 1, 1981
ReceivedApr 17, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K811066

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.