# K231225: EConsole1

- Pathway: 510(k) (Traditional)
- Applicant: DRTECH Corporation
- Decided: Oct 18, 2023 after 173 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K896095 (1990). 10 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110033: Feel-DRCS, Imfou Co., Ltd. (2011) Summary page 4.

## Most influential descendants
- K251410: VXvue (2025), 0 descendants of its own
- K241425: AspenView (2025), 0 descendants of its own
- K240243: EConsole2 (2024), 0 descendants of its own

## Indications for use
EConsole1 is indicated for use in general radiographic images of human anatomy. It is intended to replace radiographic film/screen systems in all general-purpose diagnostic procedures (excluding fluoroscopic, angiographic, and mammographic applications). The main features of this software are controlling and interfacing the detector, controlling the x-ray generator acquisition settings, storing acquired images, data management and image processing.

Source page: https://510kreport.com/device/K231225
Methodology: https://510kreport.com/methodology