# K140729: Aplio Artida, V3.2

- Pathway: 510(k) (Traditional)
- Applicant: Toshiba America Medical Systems, In.C
- Decided: May 23, 2014 after 60 days
- Product code: IYN (System, Imaging, Pulsed Doppler, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1550
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 13 generations back to K894632 (1989). 62 ancestors in all.
28 later devices descend from it; 2 cite it directly.
0 of 91 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121577: Aplio Artida Diagnostic Ultrasound System, Toshiba Medical Systems Corporation, Japan (2012) Summary page 1.

## Most influential descendants
- K173090: Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4 (2018), 21 descendants of its own
- K182679: Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V3.1 (2018), 10 descendants of its own
- K191467: Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V4.0 (2019), 9 descendants of its own
- K201972: Aplio i900/i800/i700 Diagnostic Ultrasound System, Software V5.1 (2020), 7 descendants of its own
- K212333: Aplio i900/i800/i700 Diagnostic Ultrasound System, Software V6.5 (2022), 6 descendants of its own

## Indications for use
The DIAGNOSTIC ULTRASOUND SYSTEM APLIO ARTIDA (Model SSH-8800V) is intended to be used for the following types of studies: cardiac, transesophageal, abdominal and peripheral vascular.

Source page: https://510kreport.com/device/K140729
Methodology: https://510kreport.com/methodology