Shenzhen Ruiyi Business Technology Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2024-11-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232965 | Leg Massager (Models:RP-ALM070H, RP-ALM071H) | IRP | 2024-11-20 | View |
| 510(k) | K222924 | Leg Massager RF-ALM070 | IRP | 2022-12-23 | View |
No matching devices.