K251000
- 510(k) number
- K251000
- Device name
- Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)
- Applicant
- Shenzhen Chuangtong Yigou Technology Co., Ltd. CN
- Product code
- OHT — Light Based Over-The-Counter Hair Removal
- Decision date
- 2025-06-30
- Date received
- 2025-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K251000.pdf
Official FDA record: K251000
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.