Nanjing Vishee Medical 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 |
|---|
| K230767 | Pelvic Floor Muscle Stimulator | September 21, 2023 |
| K222875 | Powered Muscle Stimulator (Model name:MagGraver F200) | March 9, 2023 |