# K032477: GE Logiq Book

- Pathway: 510(k) (Traditional)
- Applicant: General Electric Co.
- Decided: Oct 22, 2003 after 71 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: 4 generations back to K863700 (1987). 4 ancestors in all.
666 later devices descend from it; 1 cites it directly.
2 of 671 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K014206: Logiqbook, General Electric Co. (2002)

## Most influential descendants
- K050126: GE Logiq Twin (2005), 665 descendants of its own
- K072797: GE Logiq I Comapact Ultrasound, GE Logiq E Compact Ultrasound, GE Vivid E Compact Ultrasound (2007), 664 descendants of its own
- K091164: GE Venue 40, Model 5324338 (2009), 605 descendants of its own
- K091374: GE Logiq I/E & Vivid E Compact Ultrasound (2009), 521 descendants of its own
- K102256: GE Logiq I/E & Vivid E Compact Diagnostic Ultrasound (2010), 511 descendants of its own

## Indications for use
The GE LOGIQ Book BT03 is a general purpose ultrasound system. Specific clinical uses include FetaVOB; Abdominal (GYN & Urology); Pediatric; Small Organ (breast, testes, thyroid); Neonatal and Adult Cephalic; Cardiac (adult & pediatric); Peripheral Vascular; Intra-operative (abdominal, thoracic and PV), Musculo-skeletal Conventional; Transrectal; and Transvaginal.

Source page: https://510kreport.com/device/K032477
Methodology: https://510kreport.com/methodology