510(k) K192432
K192432 is an FDA 510(k) premarket notification submitted by Shenzhen Bosidin Technology Co., Ltd. for the device "IPL Home Use Hair Removal Device Model(s): D-1128, D-1103, D-1119, D-1129, D-1130". The FDA issued a decision of Substantially Equivalent on Nov 8, 2019. The device falls under product code OHT (Light Based Over-The-Counter Hair Removal), a Class II device regulated under 21 CFR 878.4810.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 8, 2019
- Date Received
- Sep 5, 2019
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Light Based Over-The-Counter Hair Removal
- Device Class
- Class II
- Regulation Number
- 878.4810
- Review Panel
- SU
- Submission Type
- 510(k)
Over-the-counter device uses thermal energy to kill hair follicles for hair removal.