# K102104: GE Vivid P3 Diagnostic Ultrasound Imaging System

- Pathway: 510(k) (Special)
- Applicant: Wipro GE Healthcare Private, Ltd.
- Decided: Oct 1, 2010 after 66 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: 7 generations back to K863700 (1987). 16 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072797: GE Logiq I Comapact Ultrasound, GE Logiq E Compact Ultrasound, GE Vivid E Compact Ultrasound, General Electric Co. (2007) Summary page 2.
- K060993: GE Logiq P5 and A5, General Electric Co. (2006) Summary page 2.
- K073297: GE Logiq P6, General Electric Co. (2007) Summary page 2.
- K092079: Modification to GE Vivid S5 and S6 Diagnostic Ultrasound, Ge Medical Systems Israel, Ultrasound, Ltd. (2009) Summary page 2.

## Most influential descendants
- K112371: Logiq P3 (2011), 0 descendants of its own

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

Source page: https://510kreport.com/device/K102104
Methodology: https://510kreport.com/methodology