Data / Medical devices / China / Anhui Tianyang Pharmaceutical Co., Ltd
Anhui Tianyang Pharmaceutical Co., Ltd: FDA-registered device maker in Tianchang Anhui, China, 1 510(k) clearance
Anhui Tianyang Pharmaceutical Co., Ltd is registered with the FDA (registration 3016972038) in Tianchang Anhui, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 12, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016972038
- Address
- NO.46 Tiantong Road, Tianchang Anhui, China, 239304
- Owner or operator
- Anhui Tianyang Pharmaceutical Co., LTD. (10085731)
- Roles
- Manufacturer
- First device listed
- August 14, 2023
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Saline, Vascular Access Flush | NGT | 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 |
|---|---|---|---|---|---|---|
| August 12, 2023 | K223584 | Pre-Filled Normal Saline Flush Syringe | NGT | Substantially Equivalent | Anhui Tianyang Pharmaceutical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 12, 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.