# K112371: Logiq P3

- Pathway: 510(k) (Traditional)
- Applicant: GE Healthcare
- Decided: Sep 27, 2011 after 41 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: 10 generations back to K863700 (1987). 20 ancestors in all.
No later device cites it as a predicate yet.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102256: GE Logiq I/E & Vivid E Compact Diagnostic Ultrasound, Ge Medical Systems China Co., Ltd. (2010) Summary page 2.
- K102104: GE Vivid P3 Diagnostic Ultrasound Imaging System, Wipro GE Healthcare Private, Ltd. (2010) Summary page 2.

## Indications for use
The device is intended for use by a qualified physician for ultrasound evaluation of Fetal/Obstetrics, Abdominal (including GYN), Pediatric, Small Organ (including breast, testes, thyroid), Neonatal Cephalic, Adult Cephalic, Cardiac (adult and pediatric), Peripheral Vascular, Intraoperative (abdominal, thoracic and peripheral), Musculo-skeletal Conventional, Urology (including prostate), Transrectal and Transvaginal.

Source page: https://510kreport.com/device/K112371
Methodology: https://510kreport.com/methodology