# K233599: X-Clever (ASHK100G)

- Pathway: 510(k) (Traditional)
- Applicant: Lg Electronics.Inc
- Decided: Mar 18, 2024 after 130 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: 11 generations back to K896095 (1990). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K212137: X-Clever, Lg Electronics.Inc (2021) Summary page 6.

## Indications for use
Software used in a device that saves, enlarges, reduces, views as well as analyzes, transfers and prints medical images. (excluding fluoroscopic, angiographic, and mammographic applications.)

Source page: https://510kreport.com/device/K233599
Methodology: https://510kreport.com/methodology