ClearanceBrief
510(k) K791219 ยท DXY Implantable Pacemaker Pulse-Generator

UNILITH PULSE GENERATOR

ApplicantEla Medical, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 30, 1979
ReceivedJul 3, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791219

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.