Data / Medical devices / China / Shenzhen Antmed Co. Ltd
Shenzhen Antmed Co. Ltd: FDA-registered device maker in Dongguan Guangdong, China, 4 510(k) clearances
Shenzhen Antmed Co. Ltd is registered with the FDA (registration 3007048453) in Dongguan Guangdong, China. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated February 26, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007048453
- Address
- No.3 Hualian Ave., Songshanhu District, Dongguan Guangdong, China, 523800
- Owner or operator
- Shenzhen Antmed Co. Ltd (10025888)
- Roles
- Manufacturer
- First device listed
- May 18, 2008
- Registered through
- 2026
- Brand names listed
- ANT Angiographic Syringes, ANT Inflation Device and ANT Inflation Device Compact Pack, Disposable Pressure Transducer, Pressure Connecting Tube
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Intravascular, Diagnostic | DQO | 2 | Manufacturer | accessdata.fda.gov |
| Injector And Syringe, Angiographic | DXT | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Balloon Inflation | MAV | 2 | Manufacturer | accessdata.fda.gov |
| Transducer, Blood-Pressure, Extravascular | DRS | 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 |
|---|---|---|---|---|---|---|
| February 26, 2014 | K131770 | PRESSURE CONNECTING TUBE | DQO | Substantially Equivalent | Shenzhen Ant Hi-Tech Industrial Co., Ltd. | accessdata.fda.gov |
| July 1, 2011 | K102648 | ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK | MAV | Substantially Equivalent | Shenzhen Ant Hi-Tech Industrial Co., Ltd. | accessdata.fda.gov |
| August 18, 2009 | K091408 | DISPOSABLE PRESSURE TRANSDUCER | DRS | Substantially Equivalent | Shenzhen Ant Hi-Tech Industrial Co., Ltd. | accessdata.fda.gov |
| May 2, 2008 | K072696 | ANT ANGIOGRAPHIC SYRINGES, MODEL(S) 100101,102,103,100201,202,203,204,100301,200101,201,202, 203,200301,101,102,202,301 | DXT | Substantially Equivalent | Shenzhen Ant Hi-Tech Industrial Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Intravascular, Diagnostic
- All makers of Transducer, Blood-Pressure, Extravascular
- All makers of Injector And Syringe, Angiographic
- All makers of Syringe, Balloon Inflation
Updated February 26, 2014. 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.