Clearance Summary
RADIANCY FACIAL SKINCARE DEVICE received FDA 510(k) clearance under submission number K052991, sponsored by Radiancy (Israel) , 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 2006-02-01.
- Submission: K052991
- Applicant / Sponsor: Radiancy (Israel) , Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2006-02-01
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.