Clearance Summary
DUO received FDA 510(k) clearance under submission number K161565, sponsored by Stetic Medical Aesthetics Development (Shenzhen) 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 2016-09-01.
- Submission: K161565
- Applicant / Sponsor: Stetic Medical Aesthetics Development (Shenzhen) Co. ,Ltd
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2016-09-01
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.