Clearance Summary
Humask Pro Vision, Humask Pro Vision 3000 received FDA 510(k) clearance under submission number K222551, sponsored by Entreprise Premont, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2022-11-10.
- Submission: K222551
- Applicant / Sponsor: Entreprise Premont, Inc.
- Clearance pathway: Abbreviated
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4040
- Decision date: 2022-11-10
Classification & Regulation
This clearance is catalogued under FDA product code FXX and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.