# K143223: CGBA-032A, Aquilion PRIME Self-Propelled Scan Base Kit for IVR-CT

- Pathway: 510(k) (Traditional)
- Applicant: Toshibamedical Systems Corporation
- Decided: Jan 12, 2015 after 63 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: 9 generations back to K890348 (1989). 32 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K134025: Aquilion One Vision Self-Propelled Scan Base Kit for Ivr-CT, Toshibamedical Systems Corporation (2014) Summary page 4.
- K141741: Aquilion Prime, V6.00, Toshibamedical Systems Corporation (2014). Cleared while this submission was under review Summary page 4.
- K113052: Infinix-Cci, Toshiba America Medical Systems, In.C (2011) Summary page 4.

## Most influential descendants
- K182223: Aquilion ONE Self-Propelled Scan Base Kit for IVR-CT, CGBA-034A (2018), 1 descendant of its own
- K251645: Self-Propelled CT Scan Base Kit, CGBA-035A; Alphenix, INFX-8000C/B, INFX-8000C/S, V9.6 with Calculated DAP (2025), 0 descendants of its own

## Indications for use
Optional movable gantry base unit for use with an Aquilion PRIME system to support longitudinal movement and allow acquisition of images in the z-direction (z-axis). Note: When installed with the movable gantry base unit, Aquilion PRIME can be used with the INFX-8000C system in the same room.

Source page: https://510kreport.com/device/K143223
Methodology: https://510kreport.com/methodology