# K182836: FUJIFILM Endoscope Model EG-740N

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Corporation
- Decided: Apr 2, 2019 after 175 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: 6 generations back to K944759 (1995). 9 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063316: Fujinon Model EG-530N Trans Nasal Insertion, Fujinon, Inc. (2007) Summary page 4.
- K172916: FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/L and EC-760ZP-V/L, and FUJIFILM Water Tank Model WT-603, Fujifilm Corporation (2018) Summary page 4.

## Most influential descendants
- K240142: FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope Model EG-840TP (2024), 3 descendants of its own
- K243260: FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860R (2025), 1 descendant of its own
- K261880: FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy Support Program EW10-VM01 (2026), 0 descendants of its own
- K243512: FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope Model EG-840TP (2025), 0 descendants of its own

## Indications for use
FUJIFILM Endoscope Model EG-740N is intended for the visualization of the upper digestive tract, specifically for the observation, diagnosis, and endoscopic treatment of the esophagus, stomach, and duodenum. The device can be inserted orally or transnasally.

Source page: https://510kreport.com/device/K182836
Methodology: https://510kreport.com/methodology