Ultraviolet Phototherapy Device— 510(k) K250425
Substantially EquivalentAPK Technology Co., Ltd.
FDA 510(k) clearance K250425 for Ultraviolet Phototherapy Device, Substantially Equivalent on 2025-04-07. Applicant: APK Technology Co., Ltd..
Clearance details
- Applicant
- APK Technology Co., Ltd.
- Product code
- Code FTC
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.