Neurocareai, Inc.
Country not established
- Devices
- 3
What Neurocareai, Inc. makes
Neurocareai, Inc. manufactures the NeuroICH, a device designed for intracranial hemorrhage monitoring and assessment, enabling real-time detection and analysis of bleeding within the brain.
The NeuroICH is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
NeuroICH Ref K241719
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 066723161
Frequently asked questions
How many devices does Neurocareai, Inc. have in the registry?
The registry currently lists 3 devices for Neurocareai, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurocareai, Inc.'s devices?
Among its 3 most recently registered devices, Neurocareai, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Neurocareai, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Neurocareai, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurocareai, Inc. in the registry?
The most recently registered devices listed for Neurocareai, Inc. include NeuroICH V1.1.67, MammoSightAI 1.4.0 and NeuroICH.