K241057
- 510(k) number
- K241057
- Device name
- Enhanced Handheld Pain Relief Laser Instrument (GD-P-E)
- Applicant
- Wuhan Guangdun Technology Co.,Ltd.. CN
- Product code
- NHN — Powered Light Based Laser Non-Thermal Instrument Wit
- Decision date
- 2025-01-24
- Date received
- 2024-04-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241057.pdf
Official FDA record: K241057
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.