Eol, Inc.
Country not established
- Devices
- 1
What Eol, Inc. makes
Eol, Inc. manufactures the EOL Model LIO, a medical device designed for [specific application not detailed in provided data].
The EOL Model LIO is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Eol, Model Lio Ref K881984
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eol, Inc. have in the registry?
The registry currently lists 1 device for Eol, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eol, Inc.'s devices?
Among its 1 most recently registered device, Eol, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Eol, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eol, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eol, Inc. in the registry?
The most recently registered devices listed for Eol, Inc. include EOL, MODEL LIO.