# K060566: Minxray, Models HFP24 and HFP40

- Pathway: 510(k) (Special)
- Applicant: Mikasa X-Ray Co., Ltd.
- Decided: Apr 5, 2006 after 33 days
- Product code: IZL (System, X-Ray, Mobile)
- Device class: 2
- Regulation: 21 CFR 892.1720
- 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 K945707 (1995). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052721: Minxray, Model HF100H+, Minxray, Inc. (2005) Summary page 1.
- (no number) MinXray P200 R24/40: named in the summary without a submission number

## Indications for use
The MinXray HFP24 and HFP4O is intended for use by a qualified/trained physician or technician on both adult and pediatric subjects for taking diagnostic x-rays. These units are specifically designed for podiatric and extremity applications.

Source page: https://510kreport.com/device/K060566
Methodology: https://510kreport.com/methodology