# K041813: GE Logiq 7 Ultrasound BT04

- Pathway: 510(k) (Special)
- Applicant: Ge Medical Systems Ultrasound and Primary Care Dia
- Decided: Jul 23, 2004 after 17 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: 2 generations back to K010329 (2001). 2 ancestors in all.
630 later devices descend from it; 2 cite it directly.
0 of 633 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010329: LOGIQ 500, General Electric Co. (2001) Summary page 1.
- K032182: GE Logiq 7, Model 2354858, General Electric Co. (2003) Summary page 1.

## Most influential descendants
- K052441: GE Logiq 7 Ultrasound BT05 (2005), 629 descendants of its own
- K073408: GE Logiq BT08 Diagnostic Ultrasound System (2007), 628 descendants of its own
- K082185: GE Logiq E9 Diagnostic Ultrasound System, Models 5205000, 5205000-2 (2008), 627 descendants of its own
- K092271: GE Logiq E9 BT2010 Diagnostic Ultrasound System, Model 5205000-3, 5205000-4 (2009), 569 descendants of its own
- K110943: Logiq E9 (2011), 472 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/K041813
Methodology: https://510kreport.com/methodology