Data / Medical devices / China / Nanjing Jusha Display Technology Co., Ltd
Nanjing Jusha Display Technology Co., Ltd: FDA-registered device maker in Nanjing Jiangsu, China, 16 510(k) clearances
Nanjing Jusha Display Technology Co., Ltd is registered with the FDA (registration 3010043098) in Nanjing Jiangsu, China. It lists 7 device types. The FDA files 16 510(k) clearances under its listings, the newest dated June 9, 2023. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3010043098
- Address
- No.99 Yaogu Avenue, Nanjing Jiangbei New Area, Jiangsu Province, 210032 China., Nanjing Jiangsu, China, 210032
- Owner or operator
- Nanjing Jusha Display Technology Co., Ltd (10086870)
- Roles
- Manufacturer
- First device listed
- December 21, 2022
- Registered through
- 2026
- Brand names listed
- CR240G, E190DH1G, E190DHG, E240A1G, E240AG, E240CG, E240D1G, E240E1G and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adult Portable Bed Rails For Medical Purposes | QTC | 1 | Manufacturer | accessdata.fda.gov |
| Camera, Surgical And Accessories | KQM | 1 | Manufacturer | accessdata.fda.gov |
| Camera, Television, Surgical, Without Audio | FWB | 1 | Manufacturer | accessdata.fda.gov |
| Display, Diagnostic Radiology | PGY | 2 | Manufacturer | accessdata.fda.gov |
| Instrument, Quality-Assurance, Radiologic | LHO | 1 | Manufacturer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Manufacturer | accessdata.fda.gov |
| System, Digital Image Communications, Radiological | LMD | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 9, 2023 | K230728 | JUSHA-C810G/C810G LCD Monitor, JUSHA-C660/JUSHA-C660G/C660/C660G LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| June 7, 2023 | K231170 | C350/C350G LCD Monitor; M550/M550G LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| May 18, 2023 | K230723 | C510G/JUSHA-C510G/C510/JUSHA- C510 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| May 1, 2023 | K230643 | CP620G LCD monitor, CP620 LCD monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| September 19, 2022 | K222121 | C630G LCD monitor, JUSHA-C630G LCD monitor, C630 LCD monitor, JUSHA-C630 LCD monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| March 25, 2022 | K212231 | C1210G LCD Monitor, JUSHA-C1210G LCD Monitor, C1210 LCD Monitor, JUSHA-C1210 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| July 24, 2020 | K200742 | JUSHA-CP610 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| May 31, 2019 | K190831 | E240AG LCD Monitor, E240A LCD Monitor, JUSHA-E240AG LCD Monitor, JUJSHA-E240A LCD Monitor, C230A LCD Monitor, JUSHA-C230A LCD Monitor, C230M LCD Monitor, JUSHA-C230M LCD Monitor | GCJ | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| May 14, 2019 | K190848 | JUSHA-M550G/ JUSHA-M550/M550G/M550 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| April 8, 2019 | K183496 | JUSHA-C350G LCD Monitor, JUSHA-C350 LCD Monitor, C350G LCD Monitor, C350 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| April 5, 2019 | K183494 | R190/R191 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| March 13, 2019 | K183492 | JUSHA-C620G LCD Monitor, JUSHA-C620 LCD Monitor, C620G LCD Monitor, C620 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| February 5, 2019 | K183498 | JUSHA-C270G/ JUSHA-C270/ C270G/ C270 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| February 4, 2019 | K183499 | JUSHA-M350G/JUSHA-M350/M350G/M350 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| January 15, 2019 | K183497 | JUSHA-M260G LCD Monitor, JUSHA-M260 LCD Monitor, M260G LCD Monitor, M260 LCD Monitor | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
| April 28, 2015 | K150842 | JUSHA-M53 Medical Display | PGY | Substantially Equivalent | Nanjing Jusha Display Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Display, Diagnostic Radiology
- All makers of Camera, Television, Surgical, Without Audio
- All makers of Adult Portable Bed Rails For Medical Purposes
- All makers of Instrument, Quality-Assurance, Radiologic
- All makers of Camera, Surgical And Accessories
- All makers of System, Digital Image Communications, Radiological
Updated June 9, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.