# K172276: Xario 200 Diagnostic Ultrasound System V6.0

- Pathway: 510(k) (Traditional)
- Applicant: Toshibamedical Systems Corporation
- Decided: Dec 12, 2017 after 137 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: 19 generations back to K935595 (1995). 135 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 139 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K162155: Xario 200 Diagnostic Ultrasound System V5.0, Toshibamedical Systems Corporation (2016) Summary page 32.

## Most influential descendants
- K182596: Xario200G and Xario100G, Software V1.1 Diagnostic Ultrasound System (2018), 2 descendants of its own
- K232988: Aplio flex and Aplio go Software V2.0 Diagnostic Ultrasound System (2023), 0 descendants of its own
- K202737: Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, Aplio a550, Aplio a450, and Aplio a, Diagnostic Ultrasound System, Xario200G and Xario100G, Diagnostic Ultrasound System (2020), 0 descendants of its own

## Indications for use
The Diagnostic Ultrasound System Xario 200 Model TUS-X200 and Xario 200 Model TUS-X200S are indicated for the visualization of structures, and dynamic processes with the human body using ultrasound and to provide image information for diagnosis in the following clinical applications: fetal, abdominal, intra-operative(abdominal), laparoscopic, pediatric, small organs, neonatal cephalic, adult cephalic, trans-rectal, trans-vaginal, musculo-skeletal (conventional), musculo-skeletal(superficial), cardiac adult, cardiac pediatric, trans-esoph(cardiac) and peripheral vessel.

Source page: https://510kreport.com/device/K172276
Methodology: https://510kreport.com/methodology