# K161706: Vivid iq

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems Ultrasound and Primary Care Diagnostics L
- Decided: Aug 5, 2016 after 46 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: 21 generations back to K935595 (1995). 190 ancestors in all.
46 later devices descend from it; 6 cite it directly.
0 of 237 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121062: Vivid I Diagnostic Ultrasound System, Vivid Q Diagnostic Ultrasound System, Ge Medical System Israel, Ltd. (2012) Summary page 6.
- K150087: Vivid E80 Diagnostic Ultrasound Imaging System, Vivid E90 Diagnostic Ultrasound Imaging System, Vivid E95 Diagnostic Ultrasound Imaging System, Ge Vingmed Ultrasound AS (2015) Summary page 6.
- K160184: Voluson S6, Voluson S8, Voluson S10, GE Healthcare (2016) Summary page 6.
- K160277: LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6, GE Medical Systems Ultrasound and Primary Care Diagnostics (2016) Summary page 6.

## Most influential descendants
- K180599: Venue (2018), 28 descendants of its own
- K183362: Venue GO (2019), 14 descendants of its own
- K170878: Vivid S60N, Vivid S70N (2017), 10 descendants of its own
- K181727: Vivid iq (2018), 9 descendants of its own
- K182450: Vivid S60N, Vivid S70N (2018), 9 descendants of its own

## Indications for use
The Vivid iq is a high-performance compact ultrasound system designed for cardiovascular and shared services applications. The indications of the product will include Fetal, OB, Abdominal, Pediatric, small Organ, Neonatal Cephalic, Adult Cephalic, Cardiac, Penpheral Vascular, Musculo-skeletal Conventional, Musculo-skeletal Superficial, Transcranial, Transrectal, Transvaginal, Transesophageal, Tissue biopsy, Intraoperative, IntraCardiac and Intraluminal

Source page: https://510kreport.com/device/K161706
Methodology: https://510kreport.com/methodology