ClearanceBrief
510(k) K810489 ยท DXY Implantable Pacemaker Pulse-Generator

MULTILITH PULSE GENERATOR #1140

ApplicantEla Medical, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 29, 1981
ReceivedFeb 23, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810489

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.