# K131088: Portable Digital Color Doppler Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: Sonoscape Company Limited
- Decided: May 24, 2013 after 36 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: 1 generation back to K112602 (2011). 1 ancestor in all.
32 later devices descend from it; 3 cite it directly.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112602: S6 Diagnostic Ultrasound System, Sonoscape Company Limited (2011) Summary page 2.

## Most influential descendants
- K132768: S8 Exp Portable Digital Color Doppler Ultrasound System (2013), 30 descendants of its own
- K142710: S9 Portable Digital Color Doppler Ultrasound System (2015), 19 descendants of its own
- K150045: S30/S40 Digital Color Doppler Ultraound System (2015), 17 descendants of its own
- K152854: S50 Digital Color Doppler Ultrasound System (2016), 16 descendants of its own
- K160283: S45 Digital Color Doppler Ultrasound System (2016), 15 descendants of its own

## Indications for use
The SonoScape S9 device is a general-purpose ultrasonic imaging instrument intended for use by a qualified physician for evaluation of Fetal, Abdominal, Pediatric, Small Organ (breast, testes, thyroid), Cephalic(neonatal and adult), Trans-rectal, Trans-vaginal, Peripheral Vascular, Musculo-skeletal (Conventional and Superficial), Cardiac (neonatal and adult), OB/Gyn and Urology.

Source page: https://510kreport.com/device/K131088
Methodology: https://510kreport.com/methodology