# K143452: Logiq P9, Logiq P7

- Pathway: 510(k) (Traditional)
- Applicant: GE Healthcare
- Decided: Jan 29, 2015 after 58 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). 144 ancestors in all.
131 later devices descend from it; 3 cite it directly.
0 of 276 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141261: Logiq S7 Expert, Logiq S7 Pro, GE Healthcare (2014) Summary page 5.
- K133533: Logiq E, GE Healthcare (2014) Summary page 7.
- K141639: Voluson S6, Voluson S8, GE Healthcare (2014) Summary page 5.
- K133034: Logiq F Series, GE Healthcare (2014) Summary page 13.

## Most influential descendants
- 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
- K163596: LOGIQ P9 and LOGIQ P7 (2017), 47 descendants of its own
- K173204: RS85 Diagnostic Ultrasound System (2018), 39 descendants of its own

## Indications for use
The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superficial; Urology (including prostate); Transrectal; Transvaginal; and Intraoperative (abdominal, thoracic, vascular).

Source page: https://510kreport.com/device/K143452
Methodology: https://510kreport.com/methodology