Dolphin/XF Robot Accessory

The Dolphin/XF Robot Accessory helps acquire cerebral blood-flow velocity measurements when connected to a compatible Dolphin transcranial Doppler system. It provides positioning and…

Registry build 21.09.26

The Dolphin/XF Robot Accessory helps acquire cerebral blood-flow velocity measurements when connected to a compatible Dolphin transcranial Doppler system. It provides positioning and scanning support for the Doppler examination rather than an independent diagnostic instrument.

A dedicated headset attaches the accessory to the head for unilateral or bilateral use. Software-controlled movement scans in two angular directions, helping the user obtain the cerebral blood-flow signal through the connected Dolphin system.

Listed Item

The Dolphin/XF robot accessory, when used with the Dolphin system, is a device which assists the user in the acquisition of cerebral blood flow velocity

System Dependence

The accessory is supported by the Dolphin IQ, 4D and MAX systems. The Doppler hardware and software perform the flow-velocity measurement, while the robot supports acquisition through its controlled scanning motion.

22manufacturers in China registered for this device type
1catalogue number
3510(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 Dolphin/XF Robot Accessory
Listed by Viasonix Ltd., Israel
FDA product code IYN
Device type System, Imaging, Pulsed Doppler, Ultrasonic
Device class Class 2
Regulation 21 CFR 892.1550
Establishment Manufacturer
510(k) K202742
Record published 2021-03-31

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Distribution end date 2021-03-31

Catalogue Numbers

Catalogue numbers for Dolphin/XF Robot Accessory
Catalogue number Size Status
Dolphin/XF Robot Accessory Withdrawn

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
K202742 2021-01-25
K191023 2019-05-16
K170859 2017-11-14

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