# K203042: Aquilion Exceed LB (TSX-202A/3) V10.6 with AiCE-I

- Pathway: 510(k) (Traditional)
- Applicant: Canon Medical Systems Corporation
- Decided: Dec 10, 2020 after 65 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K093891 (2010). 10 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192832: Aquilion Prime SP (TSX-303B8) V10.2 with AiCE-i, Canon Medical Systems Corporation (2020) Summary page 5.

## Most influential descendants
- K211828: Aquilion Exceed LB (2021), 0 descendants of its own

## Indications for use
This device is indicated to acquire and display cross-sectional volumes of the whole body, to include the head. The Aquilion Exceed LB has the capability to provide volume sets. These volume sets can be used to perform specialized studies, using indicated software/hardware, by a trained and qualified physician. AiCE (Advanced Intelligent Clear-IQ Engine) is a noise reduction algorithm that improves image quality and reduces image noise by employing Deep Convolutional Neural Network methods for abdomen, pelvis, lung, extremities, head and inner ear applications.

Source page: https://510kreport.com/device/K203042
Methodology: https://510kreport.com/methodology