K242440
- 510(k) number
- K242440
- Device name
- Intense Pulsed Light Treatment System (LK-PT)
- Applicant
- Nanjing Bestview Laser S&T Co., Ltd. CN
- Product code
- ONF — Powered Light Based Non-Laser Surgical Instrument Wi
- Decision date
- 2024-11-14
- Date received
- 2024-08-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K242440.pdf
Official FDA record: K242440
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.