Electromyograph, diagnostic
FDA product code IKN · Class 2 · 6 devices · 11 reports · 0 devices named in recalls
- Neuropack S1 DC-940BANihon Kohden Corporation · Electromyograph, diagnostic4 reports
- Natus 515-015300Natus Neurology Incorporated · Electromyograph, Diagnostic3 reports
- Natus 515-016200Natus Neurology Incorporated · Electromyograph, Diagnostic1 report
- NVM5 1559165Nuvasive, Inc. · Electromyograph, diagnostic1 report
- PULSE 50120104Nuvasive, Inc. · Electromyograph, diagnostic1 report
- NA 8225490Medtronic Xomed, Inc. · Electromyograph, diagnostic1 report