ClearanceBrief
510(k) K790098 ยท DXY Implantable Pacemaker Pulse-Generator

ISOLATION SLEEVE, MODEL 349-01

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 24, 1979
ReceivedJan 16, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790098

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.