Clearance Summary
Diosculpt received FDA 510(k) clearance under submission number K222265, sponsored by Shanghai Wonderful Opto-Electrics Tech.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 2022-09-23.
- Submission: K222265
- Applicant / Sponsor: Shanghai Wonderful Opto-Electrics Tech.Co.,Ltd
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.5400
- Decision date: 2022-09-23
Classification & Regulation
This clearance is catalogued under FDA product code PKT and 21 CFR 878.5400, within the General, Plastic Surgery review panel as a Class II device.