510(k) K251034

Device
Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)
Applicant
Shenzhen Nuon Medical Equipment Co., Ltd.
510(k) number
K251034
Product code
NFO
Decision
Substantially Equivalent (SESE)
Decision date
2025-10-12
Date received
2025-04-03
Regulation
882.5890
Classification name
Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Alain Dijkstra
Address
1st Floor-3rd Floor,# 27-2,Xintang Rd.,Xintian Community Fuhai St.,Baoan District Shenzhen CN 518000 518000

FDA Registration Numbers

Source Documents

510(k) summary PDF

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