K251034
- 510(k) number
- K251034
- Device name
- Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)
- Applicant
- Shenzhen Nuon Medical Equipment Co., Ltd. CN
- Product code
- NFO — Stimulator, Transcutaneous Electrical, Aesthetic Pur
- Decision date
- 2025-10-12
- Date received
- 2025-04-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
510(k) Summary (official FDA PDF): K251034.pdf
Official FDA record: K251034
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.