Huizhou Xinyi 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 |
| K240981 | Air compression leg massager | August 2, 2024 |
| K221862 | YY-A02-B Overlapped Compression Therapy | December 8, 2022 |