510(k) K240360
K240360 is an FDA 510(k) premarket notification submitted by Shenzhen Qianyu Technology Co., Ltd. for the device "Wrinkle Treatment Device (JM2)". The FDA issued a decision of Substantially Equivalent on Apr 5, 2024. The device falls under product code OHS (Light Based Over The Counter Wrinkle Reduction), a Class II device regulated under 21 CFR 878.4810. Shenzhen Qianyu Technology Co., Ltd. has 6 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 5, 2024
- Date Received
- Feb 6, 2024
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Light Based Over The Counter Wrinkle Reduction
- Device Class
- Class II
- Regulation Number
- 878.4810
- Review Panel
- SU
- Submission Type
- 510(k)
Use of light based treatment to reduce wrinkles on the body in general or specific anatomical locations depending on the information provided.