# K252996: Universal 1417PI

- Pathway: 510(k) (Abbreviated)
- Applicant: Konica Minolta Healthcare Americas, Inc.
- Decided: Jun 12, 2026 after 267 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- 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: 15 generations back to K896095 (1990). 27 ancestors in all.
No later device cites it as a predicate yet.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K214030: Universal DR 1748, Konica Minolta Healthcare Americas, Inc. (2022) Summary page 5.

## Indications for use
This device is indicated for use in generating radiographic images of human anatomy. It is intended to a replace radiographic film/screen system in general-purpose diagnostic procedures. This device is not indicated for use in mammography, fluoroscopy, and angiography applications.

Source page: https://510kreport.com/device/K252996
Methodology: https://510kreport.com/methodology