ClearanceBrief
510(k) K772051 ยท DXY Implantable Pacemaker Pulse-Generator

MDL-201

ApplicantPacesetter Systems, Mchenry IL, US
DecisionSubstantially Equivalent, Jan 30, 1978
ReceivedOct 31, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772051

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.