Neurotron Inc
United Statesfrom the FDA registration address FDA establishment FEI 1121806
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Neurometer Ref K853608
Regimes: 510(k) Registry: 510(k)Digital Electroneurometer S-100 Ref K843924
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1121806
- Address
- 12635 East Montview Blvd, Aurora, CO, 80045
Frequently asked questions
How many devices does Neurotron Inc have in the registry?
The registry currently lists 3 devices for Neurotron Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurotron Inc's devices?
Among its 3 most recently registered devices, Neurotron Inc has devices listed in FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Neurotron Inc's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Neurotron Inc's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurotron Inc in the registry?
The most recently registered devices listed for Neurotron Inc include Neurometer® CPT/C, NEUROMETER and DIGITAL ELECTRONEUROMETER S-100.