Venus Versa System— 510(k) K152790
Substantially EquivalentVenus Concept , Ltd.
FDA 510(k) clearance K152790 for Venus Versa System, Substantially Equivalent on 2016-01-20. Applicant: Venus Concept , Ltd.. Device class: 2.
Clearance details
- Applicant
- Venus Concept , Ltd.
- Product code
- Code ONF
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sunrise, FL, US
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