# K171755: CS-series-FP with MX CFP 3131 or MX CFP 2222 Option Radiographic/Fluoroscopy System

- Pathway: 510(k) (Special)
- Applicant: Omega Medical Imaging, LLC
- Decided: Feb 9, 2018 after 241 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: 9 generations back to K912470 (1991). 25 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121293: CS-Series-FP with 3030+Option, Omega Medical Imaging, LLC (2012) Summary page 4.

## Most influential descendants
- K201172: CFP-3131, CFP-2222 (2020), 0 descendants of its own

## Indications for use
The Omega Medical Imaging, LLC CS-series-FP (SSXI) Systems are intended for use in Radiographic/fluroscopic applications including cardiac, vascular, general radiographic/fluroscopic diagnostic, and Interventional x-ray imaging.

Source page: https://510kreport.com/device/K171755
Methodology: https://510kreport.com/methodology