# K130519: Philips Uva (/09) and Philips Uva-1 (/10) Ultraviolet Lamps

- Pathway: 510(k) (Traditional)
- Applicant: Philips Lighting Company
- Decided: Dec 24, 2013 after 300 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
These are fluorescent lamps that are designed to produce ultraviolet radiation in the UV-A range. They are not marketed with any additional components or accessories and are to be installed in fixtures designed for treatment of dermatological conditions. The intended function of these UV-A ultraviolet lamps is to be installed in the appropriate devices used for therapy for various skin related disorders.

Source page: https://510kreport.com/device/K130519
Methodology: https://510kreport.com/methodology