Data / Medical devices / China / Weipeng (suzhou) Medical Devices Co., Ltd.
Weipeng (suzhou) Medical Devices Co., Ltd.: FDA-registered device maker in Suzhou Jiangsu, China, 1 510(k) clearance
Weipeng (suzhou) Medical Devices Co., Ltd. is registered with the FDA (registration 3018884581) in Suzhou Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 7, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018884581
- Address
- 218 Xinghu St. Unit 207, Building B2, BIOBAY, Suzhou Jiangsu, China, 215123
- Owner or operator
- Weipeng (Suzhou) Medical Devices Co., Ltd. (10083897)
- Roles
- Manufacturer
- First device listed
- December 28, 2021
- Registered through
- 2026
- Brand names listed
- AcuSee AS-P1000 System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 2 | 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 |
|---|---|---|---|---|---|---|
| October 7, 2020 | K202119 | AcuSee AS-P1000 System | IYO | Substantially Equivalent | Weipeng (Suzhou) Medical Devices Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 7, 2020. 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.