# K081585: Endoscopy Video Camera System

- Pathway: 510(k) (Special)
- Applicant: Vision Systems Group, A Division of Viking Systems
- Decided: Jun 20, 2008 after 15 days
- Product code: FET (Endoscopic Video Imaging System/Component, 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: 1 generation back to K941919 (1994). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K941919: Oktas Endoscopy Video Camera System, Oktas (1994) Summary page 1.

## Most influential descendants
- K101810: 3DHJD Camera System Model (2010), 0 descendants of its own

## Indications for use
The Endoscopy Video Camera System is for use during diagnostic and/or surgical procedures when endoscopic video assistance is required.

Source page: https://510kreport.com/device/K081585
Methodology: https://510kreport.com/methodology
