# K221238: FUJIFILM Ultrasonic Endoscope EG-740UT

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Corporation
- Decided: Aug 19, 2022 after 112 days
- Product code: ODG (Endoscopic Ultrasound System, Gastroenterology-Urology)
- 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: 9 generations back to K822846 (1982). 28 ancestors in all.
No later device cites it as a predicate yet.
1 of 29 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183433: FUJIFILM Ultrasonic Endoscope, Fujifilm Corporation (2019) Summary page 4.

## Indications for use
FUJIFILM Ultrasonic Endoscope EG-740UT is intended to provide ultrasonic images of submucosal and peripheral organs of the upper gastrointestinal tract for observation, diagnosis, and endoscopic treatment. This product is intended to be used with a FUJIFILM ultrasonic processor. This product is not intended for use on children and infants.

Source page: https://510kreport.com/device/K221238
Methodology: https://510kreport.com/methodology