# K141768: Logiq V5/Logiq V3

- Pathway: 510(k) (Traditional)
- Applicant: GE Healthcare
- Decided: Aug 4, 2014 after 34 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: 18 generations back to K935595 (1995). 127 ancestors in all.
57 later devices descend from it; 3 cite it directly.
0 of 185 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133034: Logiq F Series, GE Healthcare (2014) Summary page 7.
- K131267: Voluson E6/E8/E8EXPERT/E8EXPERT Limited Edition/E10, GE Healthcare (2013) Summary page 11.

## Most influential descendants
- K160277: LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 (2016), 47 descendants of its own
- K161706: Vivid iq (2016), 46 descendants of its own
- K180599: Venue (2018), 28 descendants of its own
- K183362: Venue GO (2019), 14 descendants of its own
- K161224: LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 (2016), 11 descendants of its own

## Indications for use
The LOGIQ V5/LOGIQ V3 is general purposed ultrasound imaging and analysis systems providing digital acquisition, processing and display capability and clinical applications including: Abdominal, Obstetrical, Gynecological, Small parts, Vascular/Peripheral Vascular, Adult Cephalic, Pediatric, Musculoskeletal, Transcranial, Neonatal Cephalic, Transvaginal, Urological and Cardiac.

Source page: https://510kreport.com/device/K141768
Methodology: https://510kreport.com/methodology