# K091305: Clearpath

- Pathway: 510(k) (Traditional)
- Applicant: Easyglide, Ltd.
- Decided: Oct 23, 2009 after 172 days
- Product code: FDF (Colonoscope 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: 5 generations back to K921244 (1992). 25 ancestors in all.
13 later devices descend from it; 4 cite it directly.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032688: Colonosight Model 510B, Sightline Technologies, Ltd. (2004) Summary page 1.
- K031773: Endo Gator System, Byrne Medical, Inc. (2003) Summary page 1.
- K000948: Olympus Endoscopic Flushing Pump Model Ofp-1, Keymed (Medical & Industrial Equipment), Ltd. (2000) Summary page 1.

## Most influential descendants
- K093779: Clearpath Ugi (2010), 10 descendants of its own
- 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

## Indications for use
The ClearPath is intended to connect to standard colonoscopes to help facilitate intra-procedural cleaning of a poorly prepared colon by irrigating or cleaning the colon and evacuating the irrigation fluid (water) and feces. It is for use only by trained medical personnel located in hospitals, clinics, and doctors' offices.

Source page: https://510kreport.com/device/K091305
Methodology: https://510kreport.com/methodology