Alfred V. Greco
Country not established
- Devices
- 1
What Alfred V. Greco makes
Alfred V. Greco manufactures the EGS Model 300, an electrographic stimulator designed for neuromodulation applications.
The EGS Model 300 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Egs Model 300 Ref K790847
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alfred V. Greco have in the registry?
The registry currently lists 1 device for Alfred V. Greco. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alfred V. Greco's devices?
Among its 1 most recently registered device, Alfred V. Greco has devices listed in FDA 510(k) (1 device).
What risk classes do Alfred V. Greco's devices fall under?
Among its 1 most recently registered device, the classes recorded for Alfred V. Greco's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alfred V. Greco in the registry?
The most recently registered devices listed for Alfred V. Greco include EGS MODEL 300.