ClearanceBrief
510(k) K770211 ยท DXY Implantable Pacemaker Pulse-Generator

MICROPULSE MODEL 20S

ApplicantEdwards Pacemaker Systems, Mchenry IL, US
DecisionSubstantially Equivalent, Mar 7, 1977
ReceivedJan 31, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770211

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.