K242700
- 510(k) number
- K242700
- Device name
- Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-59C, HD-59D, HD-70, HD-72, HD-72A, HD-73A, HD-73B, HD-116, HD-116A, HD-53A, HD-53B)
- Applicant
- Shenzhen Nuon Medical Equipment Co., Ltd. CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2024-12-19
- Date received
- 2024-09-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.7 MB · U.S. public domain
Also available from FDA: K242700.pdf
Official FDA record: K242700
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.