# K932771: Battery Powered, Disposable Endoscope Light Source

- Pathway: 510(k) (Traditional)
- Applicant: Xomed-Treace, Inc.
- Decided: Aug 24, 1994 after 442 days
- Product code: EQH (Source, Carrier, Fiberoptic Light)
- Device class: 1
- Regulation: 21 CFR 874.4350
- 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; 1 cites 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
- K960081: Battery Powered Endosccopic Light Source (1996), 7 descendants of its own
- K042381: Coronary Sinus Visualization System, Model CSVS5508 (2004), 3 descendants of its own
- K020889: Endoscopic Light Source XL202/L3 (2002), 2 descendants of its own
- K050808: Coronary Sinus Access Kit, Model KCS8F-01 (2005), 1 descendant of its own
- K023468: Endoscopic Light Source XL180/L3 (2003), 1 descendant of its own

Source page: https://510kreport.com/device/K932771
Methodology: https://510kreport.com/methodology