Beijing Honkon Technologies Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K161892 | Slimming Treatment Device | March 2, 2017 |
| K131838 | DIODE LASER FOR HIAR REMOVAL | April 24, 2014 |
| K131837 | CO2 FRACTIONAL LASER | January 22, 2014 |
| K131857 | Q-SWITCHED ND:YAG LASER | January 16, 2014 |
| K131859 | MULTIFUNCTIONAL SERIES | October 18, 2013 |