# K161224: LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
- Decided: Aug 5, 2016 after 98 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: 19 generations back to K935595 (1995). 128 ancestors in all.
11 later devices descend from it; 1 cites it directly.
0 of 140 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141768: Logiq V5/Logiq V3, GE Healthcare (2014) Summary page 4.

## Most influential descendants
- K180995: Vscan Extend (2018), 10 descendants of its own
- K202035: Vscan Air (2020), 3 descendants of its own
- K181934: Vivid T8, Vivid T9 (2018), 3 descendants of its own
- K200851: Vivid T8, Vivid T9 (2020), 2 descendants of its own
- K231301: Vscan Air (2023), 1 descendant of its own

## Indications for use
The LOGIQ V5 Expert / LOGIQ V5 / LOGIQ V3 are 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, Cardiac, Transrectal, and Tissue Biopsy/Fluid Drainage.

Source page: https://510kreport.com/device/K161224
Methodology: https://510kreport.com/methodology