# K131131: E.G. Scan (TM) II Esophagoscope System

- Pathway: 510(k) (Special)
- Applicant: Intromedic Co., Ltd.
- Decided: Jun 21, 2013 after 60 days
- Product code: EOX (Esophagoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4710
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K921244 (1992). 20 ancestors in all.
No later device cites it as a predicate yet.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120702: E.G. Scan II Esphagoscope System, Intromedic Co., Ltd. (2012) Summary page 1.

## Indications for use
E.G. Scan™ |l Esophagoscope System is Intended for use in endoscopic access and examination of the larynx, esophagus and gastroesophageal junction.

Source page: https://510kreport.com/device/K131131
Methodology: https://510kreport.com/methodology