Telesystems Co., Ltd.
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- Devices
- 1
What Telesystems Co., Ltd. makes
Telesystems Co., Ltd. makes the QMASTER-H/REVO device.
The QMASTER-H/REVO is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Qmaster-H/Revo Ref K133797
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Telesystems Co., Ltd. have in the registry?
The registry currently lists 1 device for Telesystems Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telesystems Co., Ltd.'s devices?
Among its 1 most recently registered device, Telesystems Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Telesystems Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Telesystems Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Telesystems Co., Ltd. in the registry?
The most recently registered devices listed for Telesystems Co., Ltd. include QMASTER-H/REVO.