# K160277: LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems Ultrasound and Primary Care Diagnostics
- Decided: Mar 25, 2016 after 52 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). 149 ancestors in all.
47 later devices descend from it; 2 cite it directly.
0 of 197 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 17.
- K141261: Logiq S7 Expert, Logiq S7 Pro, GE Healthcare (2014) Summary page 6.
- K152758: Venue 50, GE Medical Systems Ultrasound and Primary Care Diagnostics (2015) Summary page 6.
- K141768: Logiq V5/Logiq V3, GE Healthcare (2014) Summary page 6.
- K151028: LOGIQ e, GE Medical Systems Ultrasound and Primary Care Diagnostics (2015) Summary page 6.

## Most influential descendants
- 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
- K170878: Vivid S60N, Vivid S70N (2017), 10 descendants of its own
- K181727: Vivid iq (2018), 9 descendants of its own

## Indications for use
The LOGIQ F8 Expert / LOGIQ F8 / LOGIQ F6 are general purpose ultrasound imaging and analysis systems providing digital acquisition, processing and display capability, clinical applications including: Abdominal, Obstetrical, Gynecological, Small parts, Vascular/Peripheral Vascular, Transcranial, Pediatric, Musculoskeletal, Urological, Cardiac, Transvaginal, Transrectal, and Biopsy.

Source page: https://510kreport.com/device/K160277
Methodology: https://510kreport.com/methodology