# K971416: Olympus Oes Otv-S5C Video System

- Pathway: 510(k) (Traditional)
- Applicant: Olympus America, Inc.
- Decided: Jul 16, 1997 after 91 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 K955404 (1996). 1 ancestor in all.
176 later devices descend from it; 1 cites it directly.
4 of 178 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K955404: Otv-S5 Oes Video System, Olympus America, Inc. (1996) Summary page 1.

## Most influential descendants
- K981993: Olympus Integrated Endosurgery System Endoalpha (1998), 175 descendants of its own
- K994231: Siemens Integrated Operating System (Sios) (2000), 157 descendants of its own
- K052202: Axiom Artis - Modular Angiographic System (2006), 154 descendants of its own
- K061054: Axiom Aristos FX Plus (2006), 80 descendants of its own
- K062623: Axiom Luminos DRF (2007), 78 descendants of its own

## Indications for use
Olympus Light Guide Cable A3908 is intended for use in conjunction with Olympus OTV-85C Video System and accessories with optical endoscopes for observation and recording during diagnostic and therapeutic applications requiring Type CF equipment.

Source page: https://510kreport.com/device/K971416
Methodology: https://510kreport.com/methodology