# K153059: HF1202H PowerPlus Portable X-ray Equipment

- Pathway: 510(k) (Special)
- Applicant: Minxray, Inc.
- Decided: Feb 2, 2016 after 104 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: 1 generation back to K040046 (2004). 1 ancestor in all.
17 later devices descend from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040046: Minxray, Model HF120/60H Powerplus, Minxray, Inc. (2004) Summary page 4.

## Most influential descendants
- K182207: TR90BH (2018), 16 descendants of its own
- K212144: Remex KA6 (2021), 3 descendants of its own
- K222896: AirRay (2022), 1 descendant of its own
- K210479: IMPACT and X-Ranger (2021), 1 descendant of its own
- K200637: SR-8100 Portable X-ray Unit (2020), 1 descendant of its own

## Indications for use
This radiographic system is intended for use by a qualified/trained physician or technician on both adult and pediatric subjects for taking diagnostic x-rays. Not for mammographic use.

Source page: https://510kreport.com/device/K153059
Methodology: https://510kreport.com/methodology