ClearanceBrief
510(k) K894267 ยท DXY Implantable Pacemaker Pulse-Generator

OPUS MODELS 4033 AND 4034

ApplicantEla Medical, Inc., Minnetonka MN, US
DecisionSubstantially Equivalent, Sep 20, 1989
ReceivedJun 22, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894267

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.