# K080160: Aplio Artida, Model SSH-880CV Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: Toshiba America Medical Systems, In.C
- Decided: Feb 8, 2008 after 16 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: 9 generations back to K894632 (1989). 53 ancestors in all.
181 later devices descend from it; 2 cite it directly.
0 of 235 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072826: Aplio Artida Diagnostic Ultrasound System, Toshiba America Medical Systems, In.C (2007) Summary page 1.
- K072000: Aplio XG Diagnostic Ultrasound System, Model Ssa-790A Version 2.0, Toshiba America Medical Systems, In.C (2007) Summary page 1.

## Most influential descendants
- 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
- K082596: Ultraextend Usws-900A (2008), 82 descendants of its own

## Indications for use
This device is intended to be used for the following type of studies; cardiac, transesophageal and peripheral vascular.

Source page: https://510kreport.com/device/K080160
Methodology: https://510kreport.com/methodology