# K983628: Xenon Light Source Auto Lip 5123, Model 2123.011

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Dec 11, 1998 after 57 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
Longest line of descent: 1 generation back to K952696 (1995). 1 ancestor in all.
6 later devices descend from it; 3 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K952696: Xenon Light Source Model 5121, Richard Wolf Medical Instruments Corp. (1995) Summary page 1.

## Most influential descendants
- 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
- K080809: Iec Medsight and Medbright (2008), 0 descendants of its own

## Indications for use
Light Projector AUTO LP 5123 provides light for examination, diagnostic and therapeutic applications, in particular, in endoscopy. The Xenon Light Source is classified as Cardiac Floating (CF) which permits its use for cardiac procedures when used in conjunction with the proper instrumentation for entry into the cardiac system.

Source page: https://510kreport.com/device/K983628
Methodology: https://510kreport.com/methodology