# K160857: HF 718BD X-Ray System

- Pathway: 510(k) (Traditional)
- Applicant: Arquilla, Inc. Dba X-Cel X-Ray Corporation
- Decided: Feb 24, 2017 after 332 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- 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 K811230 (1981). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K811230: X-Cell X-Ray #'S P-75W/P-75M, X-Cel X-Ray Corp. (1981) Summary page 4.

## Most influential descendants
- K231761: PodSKAN HF Diagnostic X-ray System (2023), 0 descendants of its own
- K180765: Televere Podiatry X-Ray System HF (2018), 0 descendants of its own

## Indications for use
The HF 718BD X-Ray System is intended for use by qualified clinicians for the x-ray of hands and feet.

Source page: https://510kreport.com/device/K160857
Methodology: https://510kreport.com/methodology