Kuwotech Co., Ltd.
Country not established
Part of Kuwotech
- Devices
- 1
What Kuwotech Co., Ltd. makes
Kuwotech Co., Ltd. manufactures the ZIRMON SERIES, a line of medical devices designed for specific diagnostic or therapeutic applications within Class II regulatory categorization.
The ZIRMON SERIES devices are regulated under the FDA’s 510(k) pathway and are listed in the United States. The company is based in the US.
Catalogue
Zirmon Series Ref K131117
510(k) 510(k)
Frequently asked questions
How many devices does Kuwotech Co., Ltd. have in the registry?
The registry currently lists 1 device for Kuwotech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kuwotech Co., Ltd.'s devices?
Among its 1 most recently registered device, Kuwotech Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Kuwotech Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kuwotech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kuwotech Co., Ltd. in the registry?
The most recently registered devices listed for Kuwotech Co., Ltd. include ZIRMON SERIES.