Hi-Dow International, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories3
Latest FDA decision2024-01-19
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K233461 | Hi-Dow PRO TOUCH WIRELESS 6-12 (HD-19A) | NUH | 2024-01-19 | View |
| 510(k) | K210383 | Wrap Accessory Electrodes | GXY | 2021-11-12 | View |
| 510(k) | K202337 | Pulsed electromagnetic field wrap | ILX | 2020-12-15 | View |
| 510(k) | K190617 | Wrap accessory electrodes | GXY | 2019-07-02 | View |
| 510(k) | K163393 | Hi-Dow Wireless TENS/EMS System (Model HD-5N) | NUH | 2017-08-04 | View |
No matching devices.