# K012560: GE Logiq A100 MP, Model 2272413

- Pathway: 510(k) (Special)
- Applicant: General Electric Co.
- Decided: Aug 23, 2001 after 15 days
- Product code: IYO (System, Imaging, Pulsed Echo, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1560
- 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 K863700 (1987). 2 ancestors in all.
668 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)
- K953752: RT55 Diagnostic Ultrasound System, General Electric Co. (1996) Summary page 1.

## Most influential descendants
- K014206: Logiqbook (2002), 667 descendants of its own
- K032477: GE Logiq Book (2003), 666 descendants of its own
- 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

## Indications for use
The device is intended for use by a qualified physician for ultrasound evaluation of Fetal/OB; Abdominal (GYN & Urology); Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Cardiac (adult & pediatric); Peripheral Vascular (PV); Musculo-skeletal Conventional; Transrectal (TR); and Transvaginal (TV) applications.

Source page: https://510kreport.com/device/K012560
Methodology: https://510kreport.com/methodology