Navigant Consulting, Inc.
Country not established
- Devices
- 1
What Navigant Consulting, Inc. makes
Navigant Consulting, Inc. manufactures an Electro Auricular Device, a medical device intended for use on the ear that delivers electrical stimulation for therapeutic purposes.
The Electro Auricular Device is classified as a Class U device and is listed in the FDA 510(k) registry. Navigant Consulting, Inc. is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Electro Auricular Device Ref K140530
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Navigant Consulting, Inc. have in the registry?
The registry currently lists 1 device for Navigant Consulting, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Navigant Consulting, Inc.'s devices?
Among its 1 most recently registered device, Navigant Consulting, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Navigant Consulting, Inc. in the registry?
The most recently registered devices listed for Navigant Consulting, Inc. include Electro Auricular Device.