# K951647: Welch Allyn HI - Lux Illuminator

- Pathway: 510(k) (Traditional)
- Applicant: Welch Allyn, Inc.
- Decided: May 17, 1995 after 37 days
- Product code: FCW (Light Source, Fiberoptic, Routine)
- 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
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K032430: Acueity Medical Light Source (2003), 0 descendants of its own
- K970598: Integrated Visualization System (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K951647
Methodology: https://510kreport.com/methodology