# K040046: Minxray, Model HF120/60H Powerplus

- Pathway: 510(k) (Special)
- Applicant: Minxray, Inc.
- Decided: Feb 2, 2004 after 21 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
No predicates in its family tree.
37 later devices descend from it; 5 cite it directly.
0 of 38 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) MinXray HF100H: named in the summary without a submission number

## Most influential descendants
- K153059: HF1202H PowerPlus Portable X-ray Equipment (2016), 17 descendants of its own
- K182207: TR90BH (2018), 16 descendants of its own
- K052721: Minxray, Model HF100H+ (2005), 16 descendants of its own
- K140723: Nomad MD 75K V Handheld X-Ray System (2014), 8 descendants of its own
- K212144: Remex KA6 (2021), 3 descendants of its own

## Indications for use
The MinXray HF120/60H PowerPlusTM is intended for use by a qualified/trained physician or technician on both adult and pediatric subjects for taking diagnostic x-rays.

Source page: https://510kreport.com/device/K040046
Methodology: https://510kreport.com/methodology