# K232922: Pure-Vu EVS System

- Pathway: 510(k) (Special)
- Applicant: Motus GI Medical Technologies, Ltd.
- Decided: Oct 20, 2023 after 31 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: 13 generations back to K921244 (1992). 34 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220007: Pure-Vu EVS System, Motus GI Medical Technologies, Ltd. (2022) Summary page 5.

## Most influential descendants
- K240853: Pathfinder® CR System (2024), 0 descendants of its own

## Indications for use
The Pure-Vu EVS System is intended to connect to standard or slim colonoscopes and gastroscopes to help facilitate intra-procedural cleansing of the GI tract by irrigating or cleaning and evacuating irrigation fluid (water), feces, and other bodily fluids and matter, e.g. blood. It is for use only by trained medical personnel located in hospitals, clinics and doctors’ offices.

Source page: https://510kreport.com/device/K232922
Methodology: https://510kreport.com/methodology