# K072826: Aplio Artida Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: Toshiba America Medical Systems, In.C
- Decided: Oct 24, 2007 after 21 days
- Product code: ITX (Transducer, Ultrasonic, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 892.1570
- 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 K894632 (1989). 44 ancestors in all.
182 later devices descend from it; 1 cites it directly.
0 of 227 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063130: Aplio XG Diagnostic Ultrasound System, Model Ssa-790A, Version 1.0, Toshibamedical Systems Corporation (2006) Summary page 1.
- K060542: GE Vivid 7 Model FC008XX, GE Vivid 7 Model FC009XX, General Electric Co. (2006) Summary page 1.

## Most influential descendants
- K080160: Aplio Artida, Model SSH-880CV Diagnostic Ultrasound System (2008), 181 descendants of its own
- K090158: Aplio Artida V2.0 SSH-880CV (2009), 98 descendants of its own
- K110870: Aplio Diagnostic Ultrasound System; Aplio Diagnostic Ultrasound System; Aplio Diagnostic Ultrasound System (2011), 89 descendants of its own
- K121422: Aplio 500/400/300 Diagnostic Ultrasound System (2012), 85 descendants of its own
- K123992: Aplio 500/400/300 V3.0 (2013), 82 descendants of its own

## Indications for use
The Aplio ARTIDA is intended to be used to display cardiac images.

Source page: https://510kreport.com/device/K072826
Methodology: https://510kreport.com/methodology