# K111049: Mobile Versa Light

- Pathway: 510(k) (Traditional)
- Applicant: Medtek Lighting Corp
- Decided: May 25, 2012 after 406 days
- Product code: FTC (Light, Ultraviolet, Dermatological)
- Device class: 2
- Regulation: 21 CFR 878.4630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K828654 (1983). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050695: Flex Controlled Phototherapy Equipment, Daavlin Distributing Co. (2005) Summary page 2.
- K872649: Hand/Foot Uva/Uvb 624-224, National Biological Corp. (1987) Summary page 2.
- K933952: Phototherapeutix Model 800B, Avex Industries, Ltd. (1995) Summary page 2.
- K031800: Solarc/Solrx 500 Series Ultraviolet Phototherapy Lamp Unit Family a New Medical Device Family Consisting of 5 Models:, Solarc Systems, Inc. (2003) Summary page 2.
- K904427: Panosol II Uvb-206, National Biological Corp. (1990) Summary page 2.

## Most influential descendants
- K134009: UV Biotek Single Panel, UV Biotek Multi-Directional (2014), 0 descendants of its own

## Indications for use
The UV Biotek Mobile-Lite model 600 is for individuals who require specific Ultraviolet radiation therapy for diagnosed skin disorders and is used for the treatment of psoriasis, vitiligo, and atopic dermatitis (eczema) on all skin types (I - VI) The UV Biotek Versa-Li te model 1400 is for individuals who require specific Ultraviolet radiation therapy for diagnosed skin disorders and is used for the treatment of psoriasis, vitiligo, and atopic dermatitis (eczema) on all skin types (I - VI)

Source page: https://510kreport.com/device/K111049
Methodology: https://510kreport.com/methodology