# K122515: C2-9-D Ultrasound Transducer

- Pathway: 510(k) (Special)
- Applicant: GE Healthcare
- Decided: Sep 11, 2012 after 25 days
- Product code: ITX (Transducer, Ultrasonic, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 892.1570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K935595 (1995). 97 ancestors in all.
No later device cites it as a predicate yet.
0 of 98 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110943: Logiq E9, GE Healthcare (2011) Summary page 1.

## Indications for use
The device is intended for use by a qualified physician for use with GE Diagnostic Ultrasound Systems for ultrasound evaluation of Fetal; Abdominal; Pediatric; Peripheral Vascular; Urology (including prostate).

Source page: https://510kreport.com/device/K122515
Methodology: https://510kreport.com/methodology