Clearance Summary
Venus Versa PRO System received FDA 510(k) clearance under submission number K232192, sponsored by Venus Concept, Inc.. 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 2023-09-11.
- Submission: K232192
- Applicant / Sponsor: Venus Concept, Inc.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2023-09-11
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.