# K101874: GE Logiq P6/P6 Pro

- Pathway: 510(k) (Special)
- Applicant: GE Healthcare
- Decided: Oct 5, 2010 after 95 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: 13 generations back to K935595 (1995). 97 ancestors in all.
221 later devices descend from it; 2 cite it directly.
0 of 319 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073297: GE Logiq P6, General Electric Co. (2007) Summary page 1.
- K092271: GE Logiq E9 BT2010 Diagnostic Ultrasound System, Model 5205000-3, 5205000-4, GE Healthcare (2009) Summary page 1.

## Most influential descendants
- K122114: Logiq S7 Expert, Logiq S7 Pro (2012), 220 descendants of its own
- K131527: Logiq S8 (2013), 219 descendants of its own
- K133034: Logiq F Series (2014), 155 descendants of its own
- K133533: Logiq E (2014), 149 descendants of its own
- K141261: Logiq S7 Expert, Logiq S7 Pro (2014), 144 descendants of its own

## Indications for use
The device is a general-purpose ultrasound system. Specific clinical applications and exam types include: Fetal; Abdominal (renal & GYN/pelvic); Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular (PV); Musculo-skeletal Conventional and Superficial; Urology (including prostate); Transesophageal (TE); Transrectal (TR); Transvaginal (TV); and Intraoperative (abdominal, thoracic, vascular and neuro).

Source page: https://510kreport.com/device/K101874
Methodology: https://510kreport.com/methodology