Clearance Summary
reVive Light Therapy® Wrinkle and Acne LED Device received FDA 510(k) clearance under submission number K223482, sponsored by Led Technologies, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2022-12-21.
- Submission: K223482
- Applicant / Sponsor: Led Technologies, Inc.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2022-12-21
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.