CBit Series Digital Color Doppler Ultrasound System

The CBit Series is a mobile diagnostic ultrasound system that acquires returning ultrasound echoes and displays anatomical images and blood-flow information. It combines a console, keyboard…

Registry build 21.09.26

The CBit Series is a mobile diagnostic ultrasound system that acquires returning ultrasound echoes and displays anatomical images and blood-flow information. It combines a console, keyboard control panel, power supply and color LCD monitor with selectable ultrasound probes.

Linear, convex and phased-array probes support different examination sites. The system provides conventional B-mode and M-mode imaging as well as Doppler modes that display or measure movement and flow.

Imaging Options

The platform includes pulsed-wave and continuous-wave Doppler, color and power Doppler, tissue Doppler, elastography and three- or four-dimensional imaging capabilities. The available examination functions depend on the probe and configuration. It is intended for clinician use across applications including abdominal, obstetric, cardiac, vascular and small-organ imaging.

22manufacturers in China registered for this device type
1catalogue number
10510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (10), Jiangsu (5), Shandong (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code IYN
Manufacturer City Province Registered as Device types
Xuzhou Yongkang Electronic Science Technology Co., Ltd. Xuzhou Jiangsu Contract manufacturer 13
Xian Friendship Medical Electronics Co., Ltd. Xi’An Shaanxi Contract manufacturer 10
Philips Ultrasound (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 5
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Contec Medical Systems Co., Ltd. Qinhuangdao Hebei Manufacturer 22
Shenzhen Viatom Technology Co., Ltd. Shenzhen Guangdong Manufacturer 9
Shantou Institute OF Ultrasonic Instruments Co., Ltd. Shantou Guangdong Contract manufacturer 8
Sonoscape Medical Corp. Shenzhen Guangdong Manufacturer 7
Carbon (Shenzhen) Medical Device Co., Ltd. Shenzhen Guangdong Manufacturer 6
Chison Medical Technologies Co., Ltd. Wuxi Jiangsu Contract manufacturer 5

Showing 12 of 22. All 22 manufacturers in China registered for System, Imaging, Pulsed Doppler, Ultrasonic

Record

Regulatory record for CBit Series Digital Color Doppler Ultrasound System
Listed by Chison Medical Technologies Co., Ltd., China
FDA product code IYN
Device type System, Imaging, Pulsed Doppler, Ultrasonic
Device class Class 2
Regulation 21 CFR 892.1550
Establishment Contract manufacturer, Manufacturer
510(k) K180974
Record published 2018-08-27
Record revised 2022-09-05 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for CBit Series Digital Color Doppler Ultrasound System
Catalogue number Size Status
CBit 8 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Hisense Qingdao Hisense Medical Co., Ltd. 219
Medisono Medisono, LLC 173
SonoScape Sonoscape Medical Corp. 111
Hisense Qingdao Hisense Medical Equipment Co., Ltd. 92
Diagnostic Ultrasound System Shenzhen Mindray BIO-Medical Electronics Co., Ltd. 89
Medistim Interconnect Cable Medistim ASA 40
Compact Cart Philips Ultrasound LLC 30
Siui Shantou Institute OF Ultrasonic Instruments Co., Ltd. 27
Clarius Ultrasound Scanner Clarius Mobile Health Corp. 25
Logiq GE Ultrasound Korea, Ltd. 25
Wisonic Shenzhen Wisonic Medical Technology Co., Ltd. 22
Vivid GE Vingmed Ultrasound A/S 21

Showing 12 of 934. All products under System, Imaging, Pulsed Doppler, Ultrasonic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253949 2026-05-22
K233697 2024-08-09
K223570 2023-03-31
K201965 2021-03-02
K201967 2021-02-26
K201968 2021-02-26
K201969 2021-02-25
K201971 2021-02-25
K200780 2020-08-05
K180974 2018-08-17

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P940005 1996-04-11 ULTRAMARK 9 HIGH DEFINITION IMAGING UULTRASOUND SYSTEM Advanced Technology Laboratories, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer