# K960081: Battery Powered Endosccopic Light Source

- Pathway: 510(k) (Traditional)
- Applicant: Mitsubishi Cable America, Inc.
- Decided: Mar 12, 1996 after 61 days
- Product code: FCQ (Light Source, Incandescent, Diagnostic)
- 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 K932771 (1994). 1 ancestor in all.
7 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)
- K932771: Battery Powered, Disposable Endoscope Light Source, Xomed-Treace, Inc. (1994) Summary page 1.

## Most influential descendants
- 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
- K070051: Acumen Insight Endocardial Visualization System (2007), 0 descendants of its own

## Indications for use
The Mitsubishi Battery Powered Endoscopic Light Source is intended for use as a light source for diagnostic endoscopes.

Source page: https://510kreport.com/device/K960081
Methodology: https://510kreport.com/methodology