K240583
- 510(k) number
- K240583
- Device name
- IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W)
- Applicant
- Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd. CN
- Product code
- OHT — Light Based Over-The-Counter Hair Removal
- Decision date
- 2024-06-18
- Date received
- 2024-03-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K240583.pdf
Official FDA record: K240583
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.