Clearance Summary
Oren LED Perioral Light Therapy System received FDA 510(k) clearance under submission number K213024, sponsored by Shenzhen Kaiyan Medical CO , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2021-12-22.
- Submission: K213024
- Applicant / Sponsor: Shenzhen Kaiyan Medical CO , Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2021-12-22
Classification & Regulation
This clearance is catalogued under FDA product code OHS and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.