# K093779: Clearpath Ugi

- Pathway: 510(k) (Traditional)
- Applicant: Easyglide, Ltd.
- Decided: Mar 9, 2010 after 90 days
- Product code: FDS (Gastroscope And Accessories, Flexible/Rigid)
- 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: 6 generations back to K921244 (1992). 27 ancestors in all.
10 later devices descend from it; 2 cite it directly.
0 of 38 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091305: Clearpath, Easyglide, Ltd. (2009) Summary page 1.
- K060907: Karl Storz Video Gastroscopes, KARL STORZ Endoscopy-America, Inc. (2006) Summary page 1.

## Most influential descendants
- K113050: Clearpath Lower GI (2012), 8 descendants of its own
- K160015: Pure Vu (2016), 7 descendants of its own
- K173392: Pure-Vu System (2017), 6 descendants of its own
- K181437: Pure Vu System (2018), 5 descendants of its own
- K191220: Pure Vu System (2019), 4 descendants of its own

## Indications for use
The ClearPath-UGI System is intended for irrigating or cleaning the upper digestive tract and evacuating the irrigation fluid, blood and bile in the upper G1 tract during endoscopic procedures. It is for use only by trained medical personnel located in hospitals, clinics, and doctors' offices.

Source page: https://510kreport.com/device/K093779
Methodology: https://510kreport.com/methodology