Data / Medical devices / China / Philips Goldway (Shenzhen) Industrial Inc.
Philips Goldway (Shenzhen) Industrial Inc.: FDA-registered device maker in SHENZHEN Guangdong, China, 1 510(k) clearance
Philips Goldway (Shenzhen) Industrial Inc. is registered with the FDA (registration 3003687189) in SHENZHEN Guangdong, China. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 27, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003687189
- Address
- No.2 Keji North 3rd Road Nan Shan District, SHENZHEN Guangdong, China, 518057
- Owner or operator
- Philips Medical Systems International BV (1217116)
- Roles
- Specification developer
- First device listed
- October 30, 2019
- Registered through
- 2026
- Brand names listed
- EarlyVue VS30 (863380), EarlyVue VS30 Vital Signs Monitor
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alarm, Blood-Pressure | DSJ | 2 | Specification developer | accessdata.fda.gov |
| Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase | CCK | 2 | Specification developer | accessdata.fda.gov |
| Cable, Transducer And Electrode, Patient, (Including Connector) | DSA | 2 | Specification developer | accessdata.fda.gov |
| Computer, Blood-Pressure | DSK | 2 | Specification developer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Specification developer | accessdata.fda.gov |
| Oximeter | DQA | 2 | Specification developer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Specification developer | 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 27, 2019 | K190624 | EarlyVue VS30 | DSJ | Substantially Equivalent | Philips Medizin Systeme Boeblingen GmbH | accessdata.fda.gov |
Compare with other makers
- All makers of Computer, Blood-Pressure
- All makers of Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Continuous Measurement Thermometer
- All makers of Alarm, Blood-Pressure
- All makers of Cable, Transducer And Electrode, Patient, (Including Connector)
Updated October 27, 2019. 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.