K251068
- 510(k) number
- K251068
- Device name
- KnoxFog Anti-fogging Device
- Applicant
- Uv One Hygienics, Inc. AZ · US
- Product code
- OCT — Anti Fog Solution And Accessories, Endoscopy
- Decision date
- 2025-08-27
- Date received
- 2025-04-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K251068.pdf
Official FDA record: K251068
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.