Shenzhen Ruiyi Business Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K232965 | Leg Massager (Models:RP-ALM070H, RP-ALM071H) | November 20, 2024 |
| K222924 | Leg Massager RF-ALM070 | December 23, 2022 |