# K002463: Stellar

- Pathway: 510(k) (Traditional)
- Applicant: Skytron, Div. the Kmw Group, Inc.
- Decided: Nov 8, 2000 after 90 days
- Product code: FSY (Light, Surgical, Ceiling Mounted)
- Device class: 2
- Regulation: 21 CFR 878.4580
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 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)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K071698: Aurora Led Series Surgical Lights (2007), 3 descendants of its own
- K100388: 21ST Century Centurion Exceled and System Two Led Lighting Systems (2010), 1 descendant of its own
- K140812: MI-750 Procedural/Minor Surgical Light (2014), 0 descendants of its own
- K083323: Nuvo Verde Led Lighting System (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K002463
Methodology: https://510kreport.com/methodology