CX20N

Catalogue number CX20PUX, listed by Wide Corporation, United States, under Display, Diagnostic Radiology. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
14510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (3), Shandong (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code PGY
Manufacturer City Province Registered as Device types
Barco (Suzhou) Healthcare Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 4
Nanjing Jusha Display Technology Co., Ltd. Nanjing Jiangsu Manufacturer 7
Qingdao Hisense Medical Equipment Co., Ltd. Qingdao Shandong Manufacturer 5
LG Electronics Nanjing New Technology Co., Ltd. Nanjing Jiangsu Manufacturer 4
Shenzhen Beacon Display Technology Co., Ltd. Shenzhen Guangdong Complaint-file establishment 2

Record

Regulatory record for CX20N
Listed by Wide Corporation, United States
FDA product code PGY
Device type Display, Diagnostic Radiology
Device class Class 2
Regulation 21 CFR 892.2050
Record published 2016-09-21
Record revised 2026-07-16 (version 8)

Specifications

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

Catalogue Numbers

Catalogue numbers for CX20N
Catalogue number Size Status
CX20PUX In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
RadiForce® Eizo Corporation 108
Beacon Shenzhen Beacon Display Technology Co., Ltd. 33
JVC JVC Kenwood Corporation 20
Nio Color 3MP Barco, Inc 18
Jusha Nanjing Jusha Display Technology Co., Ltd. 16
Nio Color 2MP Barco, Inc 14
Totoku JVC Kenwood Corporation 11
LG LG Electronics Inc. 11
Nio 5.8MP Gray Barco, Inc 8
Hisense Qingdao Hisense Medical Equipment Co., Ltd. 7
Coronis Fusion 4MP Barco, Inc 7
Coronis Fusion 6MP Barco, Inc 6

Showing 12 of 40. All products under Display, Diagnostic Radiology

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K222719 2023-05-09
K222716 2023-05-08
K222717 2022-10-31
K222722 2022-10-31
K210493 2021-04-14
K210491 2021-04-08
K170781 2017-04-04
K170783 2017-03-31
K160354 2016-05-02
K160353 2016-04-22
K160346 2016-04-14
K160348 2016-04-14
K160351 2016-04-07
K160355 2016-04-07

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