Clearance Summary
Diode laser hair removal machine (QDTM-04) received FDA 510(k) clearance under submission number K261693, sponsored by Beijing Nubway S&T 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 2026-07-17.
- Submission: K261693
- Applicant / Sponsor: Beijing Nubway S&T Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2026-07-17
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.