ClearanceBrief
510(k) K802407 ยท DTD Pacemaker Lead Adaptor

PACEMAKER LEAD ADAPTOR MODEL 431

ApplicantPacesetter Systems, Mchenry IL, US
DecisionSubstantially Equivalent, Oct 31, 1980
ReceivedOct 3, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802407

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.