Clearance Summary
Intense Pulsed Light Equipment received FDA 510(k) clearance under submission number K220385, sponsored by Beijing Globalipl Development 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 2022-08-12.
- Submission: K220385
- Applicant / Sponsor: Beijing Globalipl Development Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2022-08-12
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.