# K023899: Dual Yellow Laser, Model D10B

- Pathway: 510(k) (Traditional)
- Applicant: Norseld Pty., Ltd.
- Decided: Feb 20, 2003 after 90 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- 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 K883541 (1988). 5 ancestors in all.
3 later devices descend 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)
- K013940: Laser System Yellowstar, Asclepion-Meditec AG (2002)

## Most influential descendants
- K032397: Dual Yellow Laser, Model Dual Yellow D10B (2004), 2 descendants of its own
- K132976: Advatx (2014), 1 descendant of its own
- K250189: AdvaTx (2025), 0 descendants of its own

## Indications for use
The Dual Yellow Laser is intended for the treatment of vascular and pigmented lesions.

Source page: https://510kreport.com/device/K023899
Methodology: https://510kreport.com/methodology