# K113166: Clearpath Upper GI

- Pathway: 510(k) (Special)
- Applicant: Easyglide, Ltd.
- Decided: May 16, 2012 after 202 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: 7 generations back to K921244 (1992). 28 ancestors in all.
No later device cites it as a predicate yet.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093779: Clearpath Ugi, Easyglide, Ltd. (2010) Summary page 1.

## Indications for use
The ClearPath Upper GI is intended for irrigating or cleaning the upper digestive tract and evacuating the irrigation fluid, blood and bile in the upper GI 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/K113166
Methodology: https://510kreport.com/methodology