Oxford Brain Diagnostics, Ltd.
United KingdomFDA 510(k) applicant, unverified FDA FEI 3035386366
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- GUDID
CDM Insights Ref K240680
510(k) 510(k)
Company details
- FDA FEI number
- 3035386366
- DUNS number
- 224552649
- Address
- Blue Boar Court, Oxford
Frequently asked questions
How many devices does Oxford Brain Diagnostics, Ltd. have in the registry?
The registry currently lists 2 devices for Oxford Brain Diagnostics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oxford Brain Diagnostics, Ltd.'s devices?
Among its 2 most recently registered devices, Oxford Brain Diagnostics, Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Oxford Brain Diagnostics, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Oxford Brain Diagnostics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oxford Brain Diagnostics, Ltd. in the registry?
The most recently registered devices listed for Oxford Brain Diagnostics, Ltd. include CDM Insights 1.53 and CDM Insights.