ClearanceBrief
510(k) K771670 ยท DXY Implantable Pacemaker Pulse-Generator

IMPLANTED PACEMAKER PLUSE GENERATOR

ApplicantTelectronics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 12, 1977
ReceivedSep 1, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K771670

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.