Transamerican Medical Imaging
Country not established
- Devices
- 1
What Transamerican Medical Imaging makes
Transamerican Medical Imaging manufactures the SPECTRE Wireless Encrypted Footswitch and Hand Switch System, a wireless foot and hand control interface designed for medical imaging procedures. The system supports encrypted communication to enhance security and usability in radiology environments.
The SPECTRE system is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Transamerican Medical Imaging have in the registry?
The registry currently lists 1 device for Transamerican Medical Imaging. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transamerican Medical Imaging's devices?
Among its 1 most recently registered device, Transamerican Medical Imaging has devices listed in FDA 510(k) (1 device).
What risk classes do Transamerican Medical Imaging's devices fall under?
Among its 1 most recently registered device, the classes recorded for Transamerican Medical Imaging's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transamerican Medical Imaging in the registry?
The most recently registered devices listed for Transamerican Medical Imaging include SPECTRE WIRELESS ENCRYPTED FOOTSWITCH AND HAND SWITCH SYSTEM.