# K032283: Designs for Vision Fiberoptic Light

- Pathway: 510(k) (Special)
- Applicant: Designs For Vision, Inc.
- Decided: Aug 20, 2003 after 27 days
- Product code: GDB (Endoscope, Fiber Optic)
- 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: 2 generations back to K980281 (1998). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013880: Daylite Xenon Light Sources, Designs For Vision, Inc. (2001)
- K981962: Cuda Products Corp. Model M300 (M-300) Lightsource, Cuda Products Co. (1998) Summary page 1.

## Most influential descendants
- K051786: Melide Fiberoptic Light (2005), 0 descendants of its own

## Indications for use
The Designs for Vision Fiberoptic Light is indicated for use in surgery and medical applications where high intensity illumination is required

Source page: https://510kreport.com/device/K032283
Methodology: https://510kreport.com/methodology