SOLIUS PRO UVB Light Panel— 510(k) K252960
Substantially EquivalentSolius Labs, Inc.
FDA 510(k) clearance K252960 for SOLIUS PRO UVB Light Panel, Substantially Equivalent on 2026-01-16. Applicant: Solius Labs, Inc.. Device class: 2.
Clearance details
- Applicant
- Solius Labs, Inc.
- Product code
- Code SGZ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4635
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bainbridge Island, WA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.