Hebei Zhemai Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K232708 | Intense pulsed light therapy device | December 1, 2023 |
| K232709 | Diode laser therapy device | November 30, 2023 |
| K232716 | Q-Switched Nd:Yag laser | November 30, 2023 |