K241857 is an FDA 510(k) clearance for the LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293), a Light Based Over The Counter Wrinkle Reduction (Class II — Special Controls, product code OHS), submitted by Dongguan Boyuan Intelligent Technology Co.,Ltd (Dongguan, CN). The FDA issued a Cleared decision on October 11, 2024, 106 days after receiving the submission on June 27, 2024. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.
| 510(k) Number | K241857 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 27, 2024 |
| Decision Date | October 11, 2024 |
| Days to Decision | 106 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OHS — Light Based Over The Counter Wrinkle Reduction |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4810 |
| Definition | Use Of Light Based Treatment To Reduce Wrinkles On The Body In General Or Specific Anatomical Locations Depending On The Information Provided. |