Pulse-Generator, Pacemaker, External
FDA product code DTE · Class 2 · 9 devices · 4,170 reports · 6 deaths reported · 0 devices named in recalls
- NA 5392Medtronic, Inc. · PULSE-GENERATOR, PACEMAKER, EXTERNAL1 death1,934 reports
- NA 5392Medtronic, Inc. · PULSE-GENERATOR, PACEMAKER, EXTERNAL2 deaths930 reports
- NA 5392Medtronic, Inc. · PULSE-GENERATOR, PACEMAKER, EXTERNAL2 deaths654 reports
- NA 5392Medtronic, Inc. · PULSE-GENERATOR, PACEMAKER, EXTERNAL504 reports
- NA 53401Medtronic, Inc. · PULSE-GENERATOR, PACEMAKER, EXTERNAL133 reports
- SoloPace EPG SOLOEPG1Solo Pace Inc. · Pulse-Generator, Pacemaker, External5 reports
- Solo Pace Control System SOLOEPG1LSolo Pace Inc. · Pulse-Generator, Pacemaker, External5 reports
- PRO PADZ 8900-4006Zoll Medical Corporation · PULSE-GENERATOR, PACEMAKER, EXTERNAL3 reports
- 5391Oscor Inc. · PULSE-GENERATOR, PACEMAKER, EXTERNAL1 death2 reports