Seers Technology Co., Ltd.
Country not established
- Devices
- 2
What Seers Technology Co., Ltd. makes
Seers Technology Co., Ltd. manufactures the HX-461 medical device, which is classified as a Class II product.
The HX-461 is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Hx-461 Ref K120545
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seers Technology Co., Ltd. have in the registry?
The registry currently lists 2 devices for Seers Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seers Technology Co., Ltd.'s devices?
Among its 2 most recently registered devices, Seers Technology Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Seers Technology Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Seers Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Seers Technology Co., Ltd. in the registry?
The most recently registered devices listed for Seers Technology Co., Ltd. include mobiCARE Cardiac Monitoring System (mobiCARE-MC200M) and HX-461.