Clearance Summary
Accurett received FDA 510(k) clearance under submission number K161615, sponsored by H&O Equipments, Nv/Sa. 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 2016-08-23.
- Submission: K161615
- Applicant / Sponsor: H&O Equipments, Nv/Sa
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4350
- Decision date: 2016-08-23
Classification & Regulation
This clearance is catalogued under FDA product code GEH and 21 CFR 878.4350, within the General, Plastic Surgery review panel as a Class II device.