K232192
- 510(k) number
- K232192
- Device name
- Venus Versa PRO System
- Applicant
- Venus Concept, Inc. CA · US
- Product code
- ONF — Powered Light Based Non-Laser Surgical Instrument Wi
- Decision date
- 2023-09-11
- Date received
- 2023-07-24
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K232192.pdf
Official FDA record: K232192
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.