# K032656: GE Logiq 9 Ultrasound BT03/IQ, Model 2375600-X

- Pathway: 510(k) (Special)
- Applicant: Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc
- Decided: Oct 30, 2003 after 63 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: 2 generations back to K011188 (2001). 2 ancestors in all.
432 later devices descend from it; 2 cite it directly.
0 of 435 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011188: GE Logiq 9, Model 2188900-X, GE Medical Systems (2001)
- K030934: GE Logiq 9 Model 2375600, Ge Medical Systems, Inc. (2003) Summary page 1.

## Most influential descendants
- K040251: GE Logiq 9 Diagnostic Ultrasound System, Model 2404587 (2004), 431 descendants of its own
- K061129: GE Logiq 9, Models 2188900, 2375600, 2404587 and 5150000 (2006), 430 descendants of its own
- K082098: Sonosite Maxx Series Ultrasound System (2008), 247 descendants of its own
- K113156: Sonosite Edge Ultrasound System (2011), 216 descendants of its own
- K072164: DC-6 Diagnostic Ultrasound System (2007), 188 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 and neurosurgical).

Source page: https://510kreport.com/device/K032656
Methodology: https://510kreport.com/methodology