K261775
- 510(k) number
- K261775
- Device name
- Uv Phototherapy (KN-4001A,KN-4001B,KN-4001AB)
- Applicant
- Xuzhou Kernel Medical Equipment Co., Ltd. CN
- Decision date
- 2026-07-21
- Date received
- 2026-05-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K261775.pdf
Official FDA record: K261775
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.