ClearanceBrief
510(k) K800644 ยท DXY Implantable Pacemaker Pulse-Generator

CYBERLITH IMPLANTABLE PULSE GEN. #253-02

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 16, 1980
ReceivedMar 24, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800644

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.