Nerv Technology Inc. (D.B.A.) Fluidai Medical
CanadaFDA applicant, unverified
- Devices
- 1
What Nerv Technology Inc. (D.B.A.) Fluidai Medical makes
Fluidai Medical manufactures the Origin™, a medical device designed for minimally invasive fluid drainage and management in clinical settings, such as the treatment of hydrocephalus or cerebrospinal fluid (CSF) disorders.
The Origin™ is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Origin™ Ref K243965
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nerv Technology Inc. (D.B.A.) Fluidai Medical have in the registry?
The registry currently lists 1 device for Nerv Technology Inc. (D.B.A.) Fluidai Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nerv Technology Inc. (D.B.A.) Fluidai Medical's devices?
Among its 1 most recently registered device, Nerv Technology Inc. (D.B.A.) Fluidai Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Nerv Technology Inc. (D.B.A.) Fluidai Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Nerv Technology Inc. (D.B.A.) Fluidai Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nerv Technology Inc. (D.B.A.) Fluidai Medical in the registry?
The most recently registered devices listed for Nerv Technology Inc. (D.B.A.) Fluidai Medical include Origin™.