# K934559: Karl Storz Xenon Light Source Model 201320-20

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Apr 22, 1994 after 218 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.
4 later devices descend from it; 3 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K020889: Endoscopic Light Source XL202/L3 (2002), 2 descendants of its own
- K023468: Endoscopic Light Source XL180/L3 (2003), 1 descendant of its own
- K032545: Endoscopic Light Source LS-3000X; LS-1800XG/Med Light X 180; LS-2500H/Med Light H 250 (2003), 0 descendants of its own
- K984124: Aesculap Xenon Light Source (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K934559
Methodology: https://510kreport.com/methodology