# K120702: E.G. Scan II Esphagoscope System

- Pathway: 510(k) (Traditional)
- Applicant: Intromedic Co., Ltd.
- Decided: Jun 20, 2012 after 104 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: 7 generations back to K921244 (1992). 19 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111030: E.G. Scan (TM) Esophagoscope System, Intromedic Co., Ltd. (2011) Summary page 1.
- K072088: Flexible Trans-Nasal Video Esophagoscope with Digital Video Processor and Disposable Endosheath Systems, Vision-Sciences, Inc. (2007) Summary page 1.

## Most influential descendants
- K131131: E.G. Scan (TM) II Esophagoscope System (2013), 0 descendants of its own

## Indications for use
E.G. Scan 11 Esophagoscope System is intended for use in endoscopic access and examination of the larynx, esophagus and gastroesophageal junction.

Source page: https://510kreport.com/device/K120702
Methodology: https://510kreport.com/methodology