ClearanceBrief
510(k) K772057 ยท DXY Implantable Pacemaker Pulse-Generator

BIPOLAR PACEMAKER MODEL 224

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 3, 1977
ReceivedOct 31, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772057

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.