Well-Life Healthcare Limited
FDA 510(k) & PMA Approved Dispositivos — 8 products
Publicidad
Total de dispositivos8
Categorías0
Última decisión de la FDA
| Tipo | Número | Nombre del dispositivo | Código | Fecha | Acciones |
|---|---|---|---|---|---|
| 510(k) | K233054 | Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator; TENS/EMS WITH Menstrual Relief Stimulator; Well-Life Pain Relief Stimulator; Menstrual Plus Stimulator | NUH | 2024-10-18 | Ver |
| 510(k) | K222528 | Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe Electrode | KPI | 2022-12-29 | Ver |
| 510(k) | K220524 | Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series) | NUH | 2022-08-04 | Ver |
| 510(k) | K213091 | Well-Life TENS/EMS/Heating Stimulator | NUH | 2022-02-19 | Ver |
| 510(k) | K200942 | Well-Life Garment Electrodes (GM Series) | GXY | 2021-06-01 | Ver |
| 510(k) | K172809 | OTC Combo TENS/EMS System | NUH | 2017-10-18 | Ver |
| 510(k) | K162663 | WELL LIFE Rx Wireless TENS/EMS Stimulator, model WR-2603/2603A, WR-2604/2604A and WR-2605/2605A | GZJ | 2017-01-17 | Ver |
| 510(k) | K161453 | WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A | NUH | 2016-12-05 | Ver |
No hay dispositivos coincidentes.