Cornell Enterprises Co., Inc.
Country not established
- Devices
- 1
What Cornell Enterprises Co., Inc. makes
Cornell Enterprises Co., Inc. manufactures the Electrostimulator Model 808, a device designed for neuromuscular electrical stimulation therapy.
The Electrostimulator Model 808 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Electrostimulator Model 808 Ref K880426
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cornell Enterprises Co., Inc. have in the registry?
The registry currently lists 1 device for Cornell Enterprises Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cornell Enterprises Co., Inc.'s devices?
Among its 1 most recently registered device, Cornell Enterprises Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cornell Enterprises Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cornell Enterprises Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cornell Enterprises Co., Inc. in the registry?
The most recently registered devices listed for Cornell Enterprises Co., Inc. include ELECTROSTIMULATOR MODEL 808.