DC-80 EXP
DC-80 EXP is a mobile diagnostic ultrasound system for imaging anatomy and assessing fluid flow. It uses software-controlled acquisition and processing with linear, convex and phased-array…
DC-80 EXP is a mobile diagnostic ultrasound system for imaging anatomy and assessing fluid flow. It uses software-controlled acquisition and processing with linear, convex and phased-array probes.
Operating modes include B-mode, M-mode, pulsed and continuous-wave Doppler, color, power Doppler, tissue Doppler, three-dimensional and four-dimensional imaging, and elastography. Combined modes support different examination requirements.
Patient and Exam Range
The system is intended for adults, pregnant women, pediatric patients and neonates. Applications include abdominal, obstetric, small-organ, cephalic, musculoskeletal, cardiac, vascular and urological imaging, along with transrectal, transvaginal and transesophageal cardiac examinations.
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 | Shenzhen Mindray BIO-Medical Electronics Co., Ltd., China |
|---|---|
| FDA product code | IYN |
| Device type | System, Imaging, Pulsed Doppler, Ultrasonic |
| Device class | Class 2 |
| Regulation | 21 CFR 892.1550 |
| Establishment | Specification developer, Repacker / relabeller, Manufacturer, Exporter |
| 510(k) | K173471 |
| Record published | 2018-07-24 |
| Record revised | 2025-02-18 (version 2) |
Specifications
| MRI safety | MR Unsafe |
|---|---|
| Label carries | manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| DC-80 EXP | 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 |
|---|---|
| K260846 | 2026-05-11 |
| K253049 | 2026-02-11 |
| K251601 | 2025-12-03 |
| K251853 | 2025-11-07 |
| K251820 | 2025-09-12 |
| K251250 | 2025-09-05 |
| K251192 | 2025-08-22 |
| K250024 | 2025-05-30 |
| K250020 | 2025-05-19 |
| K250110 | 2025-05-16 |
| K242231 | 2024-11-08 |
| K241201 | 2024-09-16 |
| K241432 | 2024-09-12 |
| K240906 | 2024-07-23 |
| K240684 | 2024-06-17 |
| K240115 | 2024-04-22 |
| K231685 | 2023-10-26 |
| K230768 | 2023-06-09 |
| K222928 | 2023-02-07 |
| K221300 | 2022-09-29 |
| K221496 | 2022-09-29 |
| K220242 | 2022-03-25 |
| K220051 | 2022-03-04 |
| K212265 | 2021-11-16 |
| K212900 | 2021-11-05 |
| K211337 | 2021-07-01 |
| K210699 | 2021-06-10 |
| K210416 | 2021-06-10 |
| K203391 | 2021-03-23 |
| K201990 | 2020-11-09 |
| K201693 | 2020-08-21 |
| K200643 | 2020-07-24 |
| K200979 | 2020-05-28 |
| K200001 | 2020-04-09 |
| K200411 | 2020-04-08 |
| K200251 | 2020-04-02 |
| K192410 | 2019-12-19 |
| K192152 | 2019-12-13 |
| K183660 | 2019-04-09 |
| K183377 | 2019-04-04 |
| K190206 | 2019-03-08 |
| K182636 | 2019-01-10 |
| K181637 | 2019-01-09 |
| K182603 | 2018-11-14 |
| K180912 | 2018-07-30 |
| K173471 | 2018-01-08 |
| K172860 | 2018-01-02 |
| K172970 | 2017-10-25 |
| K171579 | 2017-10-18 |
| K171891 | 2017-09-21 |
| K171034 | 2017-07-10 |
| K163690 | 2017-04-20 |
| K170277 | 2017-03-23 |
| K162845 | 2016-12-15 |
| K162267 | 2016-09-06 |
| K161525 | 2016-07-13 |
| K160381 | 2016-03-09 |
| K152543 | 2015-10-29 |
| K152763 | 2015-10-21 |
| K152545 | 2015-10-02 |
| K150080 | 2015-06-12 |
| K150204 | 2015-04-10 |
| K143472 | 2015-01-02 |
| K141010 | 2014-05-14 |
| K140030 | 2014-02-19 |
| K132779 | 2013-11-19 |
| K132341 | 2013-08-15 |
| K130833 | 2013-06-21 |
| K130695 | 2013-06-19 |
| K123503 | 2012-12-13 |
| K122010 | 2012-07-20 |
| K121010 | 2012-04-19 |
| K120699 | 2012-04-19 |
| K113647 | 2011-12-16 |
| K110199 | 2011-02-08 |
| K103677 | 2011-01-31 |
| K103583 | 2010-12-27 |
| K100830 | 2010-05-05 |
| K083505 | 2008-12-12 |
| K083001 | 2008-10-22 |
| K081320 | 2008-05-27 |
| K080640 | 2008-03-21 |
| K063500 | 2006-12-06 |
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.