Device details
FDA 510(k) registration fields
- K number
- K234104
- Device name
- PICOANDY (Q-Switched Nd:YAG Laser)
- Company
- Wontech Co., Ltd.
- Country / region
- Korea, Republic of(KR)
- Product code
- GEX
- Device class
- Class 2
- Regulation number
- 21 CFR 878.4810
- Date received
- 2023-12-26
- Decision date
- 2024-03-15
- Submission type
- Traditional
- Technology type
- Q-Switched(AI inferred)
- Clinical applications
- Pigment treatment
- Primary application
- Pigment treatment
- Classification source
- AI classified
