San Cheong Co., Ltd.
Country not established
- Devices
- 1
What San Cheong Co., Ltd. makes
San Cheong Co., Ltd. makes a portable oxygen unit model SCA900.
This device is classified as Class I and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Portable Oxygen Unit SCA900 Ref K080243
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does San Cheong Co., Ltd. have in the registry?
The registry currently lists 1 device for San Cheong Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list San Cheong Co., Ltd.'s devices?
Among its 1 most recently registered device, San Cheong Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do San Cheong Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for San Cheong Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from San Cheong Co., Ltd. in the registry?
The most recently registered devices listed for San Cheong Co., Ltd. include PORTABLE OXYGEN UNIT SCA900.