Clearance Summary
Painless IPL System - KDT750 received FDA 510(k) clearance under submission number K220214, sponsored by Shanghai Omni Laser Skinology 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 2023-02-18.
- Submission: K220214
- Applicant / Sponsor: Shanghai Omni Laser Skinology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2023-02-18
Classification & Regulation
This clearance is catalogued under FDA product code ONF and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.