# K072075: Modification to GE Logiq A3

- Pathway: 510(k) (Special)
- Applicant: General Electric Co.
- Decided: Aug 29, 2007 after 30 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: 3 generations back to K010329 (2001). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K020263: LOGIQ 3, General Electric Co. (2002) Summary page 1.
- (no number) Logiq 200MD: named in the summary without a submission number

## Indications for use
The device is intended for use by a qualified physician for ultrasound evaluation of Fetal/OR; Abdominal (GYN & Urology); Pediatric; Small Organ (breast, testes, thyroid); Neonatal & Adult Cephalic; Cardiac (adult & pediatric); Peripheral Vascular; Musculo-skeletal (conventional & superficial); Intraoperative including neurological, Transrectal; and Transvaginal.

Source page: https://510kreport.com/device/K072075
Methodology: https://510kreport.com/methodology