Device details
FDA 510(k) registration fields
- K number
- K233237
- Device name
- xeo+ Family
- Company
- Cutera, Inc.
- Country / region
- United States(US)
- Product code
- GEX
- Device class
- Class 2
- Regulation number
- 21 CFR 878.4810
- Date received
- 2023-09-28
- Decision date
- 2023-12-15
- Submission type
- Traditional
- Technology type
- IPL(AI inferred)
- Clinical applications
- Hair removal
- Primary application
- Hair removal
- Classification source
- AI classified
