# K952696: Xenon Light Source Model 5121

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Jul 25, 1995 after 42 days
- Product code: GCT (Light Source, Endoscope, Xenon Arc)
- 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.
8 later devices descend from it; 2 cite 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K983628: Xenon Light Source Auto Lip 5123, Model 2123.011 (1998), 6 descendants of its own
- K020889: Endoscopic Light Source XL202/L3 (2002), 2 descendants of its own
- K121724: Endolight Led 1.1 Endolightled 1.2 (2012), 1 descendant of its own
- K023468: Endoscopic Light Source XL180/L3 (2003), 1 descendant of its own
- K131226: Novaprobe Led Light Source (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K952696
Methodology: https://510kreport.com/methodology