Hebei Zhemai Technology Co., Ltd.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2023-12-01
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232708 | Intense pulsed light therapy device | ONF | 2023-12-01 | View |
| 510(k) | K232716 | Q-Switched Nd:Yag laser | GEX | 2023-11-30 | View |
| 510(k) | K232709 | Diode laser therapy device | GEX | 2023-11-30 | View |
No matching devices.