Zyter, Inc.
Country not established
- Devices
- 1
What Zyter, Inc. makes
Zyter, Inc. manufactures the Zyter RPM, a remote patient monitoring device designed for tracking and transmitting vital signs data from patients to healthcare providers.
The Zyter RPM is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) premarket notification process. The company is based in the United States.
Catalogue
Zyter RPM Ref K212622
510(k) 510(k)
Frequently asked questions
How many devices does Zyter, Inc. have in the registry?
The registry currently lists 1 device for Zyter, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zyter, Inc.'s devices?
Among its 1 most recently registered device, Zyter, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Zyter, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Zyter, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zyter, Inc. in the registry?
The most recently registered devices listed for Zyter, Inc. include Zyter RPM.