Spectrum International
Country not established
- Devices
- 1
What Spectrum International makes
Spectrum International makes the PROMETEY, model G1-03, which is a medical device.
The PROMETEY, model G1-03 is a Class II device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Prometey, Model G1-03 Ref K062071
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spectrum International have in the registry?
The registry currently lists 1 device for Spectrum International. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spectrum International's devices?
Among its 1 most recently registered device, Spectrum International has devices listed in FDA 510(k) (1 device).
What risk classes do Spectrum International's devices fall under?
Among its 1 most recently registered device, the classes recorded for Spectrum International's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spectrum International in the registry?
The most recently registered devices listed for Spectrum International include PROMETEY, MODEL G1-03.