Beijing Globalipl Development Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K222916 | US 450 Diode Laser Equipment | December 9, 2022 |
| K220385 | Intense Pulsed Light Equipment | August 12, 2022 |
| K212611 | CO2 Laser Equipment | February 1, 2022 |
| K193328 | IPL + Diode Laser Machine | March 25, 2020 |