Hyper Technology, Inc.
ChinaFDA applicant, unverified
- Devices
- 1
What Hyper Technology, Inc. makes
Hyper Technology, Inc. manufactures the Hyper Source-Unit Rotating Gamma System, a medical imaging device designed for targeted radiation therapy and imaging applications.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Hyper Source-Unit Rotating Gamma System Ref K131777
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hyper Technology, Inc. have in the registry?
The registry currently lists 1 device for Hyper Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hyper Technology, Inc.'s devices?
Among its 1 most recently registered device, Hyper Technology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hyper Technology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hyper Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hyper Technology, Inc. in the registry?
The most recently registered devices listed for Hyper Technology, Inc. include HYPER SOURCE-UNIT ROTATING GAMMA SYSTEM.