510(k) K254234
K254234 is an FDA 510(k) premarket notification submitted by Choyang Medics Co., Ltd. for the device "Phototherapy System (DUV-COMBO)". The FDA issued a decision of Substantially Equivalent on May 1, 2026. The device falls under product code FTC (Light, Ultraviolet, Dermatological), a Class II device regulated under 21 CFR 878.4630.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 1, 2026
- Date Received
- December 29, 2025
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Light, Ultraviolet, Dermatological
- Device Class
- Class II
- Regulation Number
- 878.4630
- Review Panel
- SU
- Submission Type