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.. Device class: 2.
Clearance details
- Applicant
- APK Technology Co., Ltd.
- Product code
- Code FTC
- Device class
- Class 2
- Regulation
- 21 CFR 878.4630
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
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More clearances from APK Technology Co., Ltd.
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