K241857
- 510(k) number
- K241857
- Device name
- LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293)
- Applicant
- Dongguan Boyuan Intelligent Technology Co.,Ltd CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2024-10-11
- Date received
- 2024-06-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K241857.pdf
Official FDA record: K241857
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.