# K013880: Daylite Xenon Light Sources

- Pathway: 510(k) (Traditional)
- Applicant: Designs For Vision, Inc.
- Decided: Dec 7, 2001 after 14 days
- Product code: GCT (Light Source, Endoscope, Xenon Arc)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K980281 (1998). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992050: Lumenon Xenon Light Source, Walter Lorenz Surgical, Inc. (1999) Summary page 1.
- K980281: Welch Allyn Xenon 300 Light Source, Welch Allyn, Inc. (1998) Summary page 1.

## Most influential descendants
- K032283: Designs for Vision Fiberoptic Light (2003), 1 descendant of its own
- K051786: Melide Fiberoptic Light (2005), 0 descendants of its own

## Indications for use
The Daylite Xenon Light Source is indicated for use in surgery and medical applications where high intensity illumination is required

Source page: https://510kreport.com/device/K013880
Methodology: https://510kreport.com/methodology