WS80A Diagnostic Ultrasound System
The WS80A is a mobile diagnostic ultrasound system for imaging anatomy and analyzing fluid flow. It works with compatible transducers for examinations including fetal and obstetric,…
The WS80A is a mobile diagnostic ultrasound system for imaging anatomy and analyzing fluid flow. It works with compatible transducers for examinations including fetal and obstetric, abdominal, gynecological, cardiac, pediatric and peripheral vascular applications.
The system displays B and M mode images, color and spectral Doppler, tissue Doppler, harmonic imaging, three and four dimensional imaging and elastography. Operators can combine modes and measure anatomical structures using the available analysis packages.
Acoustic Output Display
Mechanical and thermal indices are displayed automatically during use to indicate acoustic output. The system processes returning ultrasound echoes into images and flow information, with measurements and calculations supporting assessment by qualified healthcare professionals.
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.
| 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
| Listed by | Samsung Medison Co., Ltd., South Korea |
|---|---|
| FDA product code | IYN |
| Device type | System, Imaging, Pulsed Doppler, Ultrasonic |
| Device class | Class 2 |
| Regulation | 21 CFR 892.1550 |
| Establishment | Manufacturer |
| 510(k) | K143089 |
| Record published | 2016-09-24 |
| Record revised | 2018-12-14 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| USS-WS8AL4K/US | In distribution | |
| USS-WS8EL4U/US | In distribution |
Same 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
| Clearance | Decision date |
|---|---|
| K261412 | 2026-07-28 |
| K254099 | 2026-03-27 |
| K252018 | 2026-01-05 |
| K250999 | 2025-07-18 |
| K243702 | 2025-02-12 |
| K242511 | 2024-12-10 |
| K242444 | 2024-11-27 |
| K241971 | 2024-10-11 |
| K240631 | 2024-06-21 |
| K240516 | 2024-06-12 |
| K233112 | 2023-12-21 |
| K231772 | 2023-10-03 |
| K230084 | 2023-04-21 |
| K223387 | 2023-02-13 |
| K221599 | 2022-08-22 |
| K220975 | 2022-06-29 |
| K221117 | 2022-06-17 |
| K220269 | 2022-05-06 |
| K220043 | 2022-04-05 |
| K211824 | 2021-09-09 |
| K211945 | 2021-09-08 |
| K210713 | 2021-07-09 |
| K210959 | 2021-06-24 |
| K210426 | 2021-05-13 |
| K210068 | 2021-04-09 |
| K202556 | 2020-10-30 |
| K200699 | 2020-05-07 |
| K200339 | 2020-04-07 |
| K192903 | 2020-01-06 |
| K192505 | 2019-12-12 |
| K192319 | 2019-12-10 |
| K192030 | 2019-09-19 |
| K191055 | 2019-06-12 |
| K191115 | 2019-06-12 |
| K190444 | 2019-05-22 |
| K182932 | 2019-02-15 |
| K182894 | 2019-01-22 |
| K182632 | 2019-01-08 |
| K182595 | 2018-12-18 |
| K181336 | 2018-12-04 |
| K180409 | 2018-05-11 |
| K173713 | 2018-03-08 |
| K173513 | 2018-02-20 |
| K173204 | 2018-02-05 |
| K171048 | 2017-08-24 |
| K171070 | 2017-08-09 |
| K172129 | 2017-08-08 |
| K170493 | 2017-03-28 |
| K163691 | 2017-02-22 |
| K153539 | 2016-10-03 |
| K162094 | 2016-08-26 |
| K153529 | 2016-02-02 |
| K153408 | 2015-12-21 |
| K152962 | 2015-11-02 |
| K151663 | 2015-08-12 |
| K150478 | 2015-03-26 |
| K143264 | 2014-12-09 |
| K143089 | 2014-11-26 |
| K142466 | 2014-10-03 |
| K141620 | 2014-07-02 |
| K133505 | 2013-12-27 |
| K133329 | 2013-11-27 |
| K132861 | 2013-10-04 |
| K130803 | 2013-04-12 |
| K122583 | 2012-09-05 |
| K113381 | 2011-12-29 |
| K112646 | 2011-10-12 |
| K112339 | 2011-08-29 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Samsung HME America, Inc. | 510(k) number | 2019-07-25 | Class II | Software design | There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode. | 5088 worldwide | 2020-09-11 |
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.
| 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.