# K963417: Vitlite (TR7700)

- Pathway: 510(k) (Traditional)
- Applicant: Escalon Trek Medical
- Decided: Dec 20, 1996 after 112 days
- Product code: MPA (Endoilluminator)
- 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.
4 later devices descend from it; 2 cite 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
- K973229: D.O.R.C. Hexon Illumination System (1997), 2 descendants of its own
- K062895: Xenon Brightstar Illumination System, Model 1266.Xiii (2006), 0 descendants of its own
- K062259: Iscience Surgical Fiberoptic Illuminator, Model FI - 100 (2006), 0 descendants of its own
- K973757: D.O.R.C. Solux Light Source (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K963417
Methodology: https://510kreport.com/methodology