# K160279: ANYVIEW-500R Fluoroscopic Mobile X-Ray System

- Pathway: 510(k) (Traditional)
- Applicant: Ecotron Co., Ltd.
- Decided: Oct 14, 2016 after 255 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: 3 generations back to K973598 (1997). 5 ancestors in all.
9 later devices descend from it; 2 cite it directly.
1 of 15 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032761: KMC-950 C-Arm Mobile System, United Radiology Systems, Inc. (2004) Summary page 5.

## Most influential descendants
- K191503: MobileRay Pulse SE Digital Imaging System (2019), 7 descendants of its own
- K211191: Virtual C DRF Digital Imaging System (2021), 5 descendants of its own
- K241567: MC2 Portable X-ray System (2024), 1 descendant of its own
- K212523: VFSS Pro Mobile Digital Imaging System (2021), 1 descendant of its own
- K212557: Virtual C DRF-NEO Digital Imaging System (2021), 1 descendant of its own

## Indications for use
Anyview-500R fluoroscopic mobile x-ray system is radiation medical equipment only used by professional radiologists. This product is designed to provide fluoroscopic and spot film images of the patient during diagnostic and interventional procedures. This system can be applied in emergency room, operation room, cast room or etc. of hospital.

Source page: https://510kreport.com/device/K160279
Methodology: https://510kreport.com/methodology