ClearanceBrief
510(k) K913134 ยท DXY Implantable Pacemaker Pulse-Generator

MODEL 4220

ApplicantPace Medical, Waltham MA, US
DecisionSubstantially Equivalent, Aug 22, 1991
ReceivedJul 16, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913134

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.