Venus Versa PRO System— 510(k) K232192
Substantially EquivalentVenus Concept, Inc.
FDA 510(k) clearance K232192 for Venus Versa PRO System, Substantially Equivalent on 2023-09-11. Applicant: Venus Concept, Inc.. Device class: 2.
Clearance details
- Applicant
- Venus Concept, Inc.
- 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
- Special
- Location
- San Jose, CA, US
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