# K133034: Logiq F Series

- Pathway: 510(k) (Traditional)
- Applicant: GE Healthcare
- Decided: Jan 31, 2014 after 127 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: 17 generations back to K935595 (1995). 125 ancestors in all.
155 later devices descend from it; 5 cite it directly.
0 of 281 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122387: Voluson P6, Voluson P8, GE Healthcare (2012) Summary page 1.
- K131527: Logiq S8, GE Healthcare (2013) Summary page 1.
- K113690: GE Logiq I, Logiq E and Vivid E, GE Healthcare (2011) Summary page 1.

## Most influential descendants
- K143452: Logiq P9, Logiq P7 (2015), 131 descendants of its own
- K161047: LOGIQ P9 and LOGIQ P7 (2016), 107 descendants of its own
- K163691: HS70A Diagnostic Ultrasound System (2017), 58 descendants of its own
- K152195: Logiq S8 (2015), 57 descendants of its own
- K141768: Logiq V5/Logiq V3 (2014), 57 descendants of its own

## Indications for use
The LOGIQ F SERIES are general purposed 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

Source page: https://510kreport.com/device/K133034
Methodology: https://510kreport.com/methodology