Wong Way Corporation
Country not established
- Devices
- 1
What Wong Way Corporation makes
Wong Way Corporation manufactures the WWMED Model 401, a medical device designed for [specific application not provided in data]. This product falls under Class II regulatory classification, indicating it is subject to special controls to ensure safety and effectiveness.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, requiring premarket notification for devices deemed substantially equivalent to predicate products. The WWMED Model 401 is listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. Wong Way Corporation is based in the United States.
Catalogue
Wwmed, Model 401 Ref K051961
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wong Way Corporation have in the registry?
The registry currently lists 1 device for Wong Way Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wong Way Corporation's devices?
Among its 1 most recently registered device, Wong Way Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Wong Way Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Wong Way Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wong Way Corporation in the registry?
The most recently registered devices listed for Wong Way Corporation include WWMED, MODEL 401.