Data / Medical devices / China / Adc Ningbo Co., Ltd.
Adc Ningbo Co., Ltd.: FDA-registered device maker in Ningbo Zhejiang, China, 5 510(k) clearances
Adc Ningbo Co., Ltd. is registered with the FDA (registration 3010262192) in Ningbo Zhejiang, China. It lists 13 device types. The FDA files 5 510(k) clearances under its listings, the newest dated March 10, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010262192
- Address
- Suite # 1406, #181, Zhongshan East Road, Ningbo Zhejiang, China, 315000
- Owner or operator
- ADC Ningbo Co., Ltd. (10046012)
- Roles
- Exporter to the US
- First device listed
- January 23, 2014
- Registered through
- 2026
- Brand names listed
- ADC
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Airway, Oropharyngeal, Anesthesiology | CAE | 1 | Exporter to the US | accessdata.fda.gov |
| Blood Pressure Cuff | DXQ | 2 | Exporter to the US | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Exporter to the US | accessdata.fda.gov |
| Fork, Tuning | GWX | 1 | Exporter to the US | accessdata.fda.gov |
| Light, Examination, Medical, Battery Powered | KYT | 1 | Exporter to the US | accessdata.fda.gov |
| Percussor | GWZ | 1 | Exporter to the US | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Exporter to the US | accessdata.fda.gov |
| Stethoscope Head | BZS | 1 | Exporter to the US | accessdata.fda.gov |
| Stethoscope, Electronic | DQD | 2 | Exporter to the US | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | Exporter to the US | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Exporter to the US | accessdata.fda.gov |
| Tape, Measuring, Rulers And Calipers | FTY | 1 | Exporter to the US | accessdata.fda.gov |
| Tourniquet, Nonpneumatic | GAX | 1 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| March 10, 2017 | K162589 | Adscope 658 Electronic Stethoscope | DQD | Substantially Equivalent | American Diagnostic Corp. | accessdata.fda.gov |
| September 11, 2006 | K061471 | MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL BP3MC1-PC | DXN | Substantially Equivalent | Microlife Intellectual Property GmbH | accessdata.fda.gov |
| February 3, 2006 | K053006 | ROSSMAX DIGITAL SPHYGMOMANOMETER MANDAUS II | DXQ | Substantially Equivalent | Rossmax Internationl , Ltd. | accessdata.fda.gov |
| January 27, 1997 | K962655 | ANEROID AND MERCURIAL SPHYGMOMANOMETERS | DXQ | Substantially Equivalent | American Diagnostic Corp. | accessdata.fda.gov |
| July 8, 1994 | K940686 | ELECTRONIC THERMOMETERS | FLL | Substantially Equivalent | American Diagnostic Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Stethoscope, Electronic
- All makers of Fork, Tuning
- All makers of Tourniquet, Nonpneumatic
- All makers of Percussor
- All makers of Continuous Measurement Thermometer
- All makers of Stethoscope Head
Updated March 10, 2017. 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.