# K112318: Clearpath 24

- Pathway: 510(k) (Traditional)
- Applicant: Promedic, Inc.
- Decided: Jun 29, 2012 after 323 days
- Product code: OCX (Endoscopic Irrigation/Suction System)
- 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). 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)
- K092429: Endogator, Byrne Medical, Inc. (2009) Summary page 1.
- K091305: Clearpath, Easyglide, Ltd. (2009) Summary page 1.
- K103239: Irrigation System, United States Endoscopy Group, Inc. (2010) Summary page 1.

## Indications for use
The ClearPath Tubing is intended to provide irrigation via irrigation fluids, such as water, during gastrointestinal endoscopic procedures when used in conjunction with the ClearPath irrigation system components (ClearPath Lower G1, ClearPath Upper G1, and ClearPath Irrigator).

Source page: https://510kreport.com/device/K112318
Methodology: https://510kreport.com/methodology