Hybridyne Imaging Technologies, Inc.
Country not established
- Devices
- 1
What Hybridyne Imaging Technologies, Inc. makes
Hybridyne Imaging Technologies, Inc. manufactures the PROXISCAN Model 101, a handheld imaging device designed for real-time, portable radiographic or fluoroscopic visualization in clinical settings.
The PROXISCAN Model 101 is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Proxiscan Model 101 Ref K093706
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hybridyne Imaging Technologies, Inc. have in the registry?
The registry currently lists 1 device for Hybridyne Imaging Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hybridyne Imaging Technologies, Inc.'s devices?
Among its 1 most recently registered device, Hybridyne Imaging Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hybridyne Imaging Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hybridyne Imaging Technologies, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hybridyne Imaging Technologies, Inc. in the registry?
The most recently registered devices listed for Hybridyne Imaging Technologies, Inc. include PROXISCAN MODEL 101.