Neuro Diagnostic Devices
Country not established
- Devices
- 1
What Neuro Diagnostic Devices makes
Neuro Diagnostic Devices manufactures the SHUNTCHECK, a device designed to detect flow in cerebrospinal fluid (CSF) shunts. It is intended for monitoring and assessing shunt functionality in patients with hydrocephalus.
The SHUNTCHECK is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Shuntcheck - Csf Shunt Flow Detector Ref K080168
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuro Diagnostic Devices have in the registry?
The registry currently lists 1 device for Neuro Diagnostic Devices. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuro Diagnostic Devices's devices?
Among its 1 most recently registered device, Neuro Diagnostic Devices has devices listed in FDA 510(k) (1 device).
What risk classes do Neuro Diagnostic Devices's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neuro Diagnostic Devices's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuro Diagnostic Devices in the registry?
The most recently registered devices listed for Neuro Diagnostic Devices include SHUNTCHECK - CSF SHUNT FLOW DETECTOR.