KnoxFog Anti-fogging Device— 510(k) K251068
Substantially EquivalentUv One Hygienics, Inc.
FDA 510(k) clearance K251068 for KnoxFog Anti-fogging Device, Substantially Equivalent on 2025-08-27. Applicant: Uv One Hygienics, Inc..
Clearance details
- Applicant
- Uv One Hygienics, Inc.
- Product code
- Code OCT
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mesa, AZ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.