# K093714: Sonoace X8 Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: Medison Co., Ltd.
- Decided: Dec 10, 2009 after 8 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: 11 generations back to K924432 (1993). 19 ancestors in all.
111 later devices descend from it; 3 cite it directly.
0 of 131 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063580: Sonoace X8 Diagnostic Ultrasound System, Medison Co., Ltd. (2006) Summary page 1.
- K092159: Accuvix V20 Diagnostic Ultrasound System, Medison Co., Ltd. (2009) Summary page 1.

## Most influential descendants
- K102065: Sonoace R7 Diagnostic Ultrasound System (2010), 110 descendants of its own
- K112646: Sonoace R7 Diagnostic Ultrasound System (2011), 108 descendants of its own
- K103722: The Sonoace R5 Diagnostic Ultrasound System (2011), 103 descendants of its own
- K113381: Mysono U6 Diagnostic Ultrasound System (2011), 102 descendants of its own
- K132228: Ugeo PT60A Diagnostic Ultrasound System (2013), 101 descendants of its own

## Indications for use
Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Source page: https://510kreport.com/device/K093714
Methodology: https://510kreport.com/methodology