ClearanceBrief
510(k) K790670 ยท DXY Implantable Pacemaker Pulse-Generator

PULSE GENERATOR MODEL 629

ApplicantElema-Schonander, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 27, 1979
ReceivedApr 6, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790670

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.