# K172700: OEC One

- Pathway: 510(k) (Traditional)
- Applicant: Ge Hualun Medical Systems Co., Ltd.
- Decided: Nov 9, 2017 after 63 days
- Product code: OWB (Interventional Fluoroscopic X-Ray System)
- Device class: 2
- Regulation: 21 CFR 892.1650
- 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 K021049 (2002). 7 ancestors in all.
3 later devices descend from it; 1 cites it directly.
2 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123603: Oec Brivo 865 Advance, Oec Brivo 785 Essential, and Oec Brivo 715 Prime, Ge Healthcare Surgery GE Oec Medical Systems, Inc. (2013) Summary page 4.

## Most influential descendants
- K182626: OEC One (2018), 2 descendants of its own
- K240828: OEC One ASD (2024), 1 descendant of its own
- K253269: OEC One CFD (2025), 0 descendants of its own

## Indications for use
The OEC One mobile C-arm system is designed to provide fluoroscopic and digital spot/film images of adult and pediatric patient populations during diagnostic, interventional, and surgical procedures. Examples of a clinical application may include: orthopedic, gastrointestinal, endoscopic, urologic, neurologic, critical care, and emergency procedures.

Source page: https://510kreport.com/device/K172700
Methodology: https://510kreport.com/methodology