# K092756: GE Vscan Compact Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: Ge Vingmed Ultrasound AS
- Decided: Sep 28, 2009 after 19 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 K935595 (1995). 63 ancestors in all.
130 later devices descend from it; 2 cite it directly.
2 of 194 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072797: GE Logiq I Comapact Ultrasound, GE Logiq E Compact Ultrasound, GE Vivid E Compact Ultrasound, General Electric Co. (2007) Summary page 1.
- K091164: GE Venue 40, Model 5324338, Ge Medical Systems China Co., Ltd. (2009) Summary page 1.
- K063761: Acuson P10 Diagnostic Ultrasound System, Siemens Medical Solutions USA, Inc. (2007) Summary page 1.

## Most influential descendants
- K102153: Mobius Ultrasound Imaging System (2011), 103 descendants of its own
- K133833: Nuvis Diagnostic Ultrasound System (2014), 87 descendants of its own
- K152899: Philips Lumify Diagnostic Ultrasound System (2015), 79 descendants of its own
- K162549: Lumify Ultrasound System (2016), 43 descendants of its own
- K151339: SONON Ultrasound Imaging System (Model: SONON 300C) (2015), 33 descendants of its own

## Indications for use
Diagnostic Ultrasound imaging, measurement and analysis of the human body as follows: Diagnostic Ultrasound imaging, measurement and analysis of the human body as follows:

Source page: https://510kreport.com/device/K092756
Methodology: https://510kreport.com/methodology