Nizar A. Mullani
Country not established
- Devices
- 1
What Nizar A. Mullani makes
Nizar A. Mullani manufactures the Nevoscope, a device designed for visualizing nerve structures during surgical procedures, aiding in precise anatomical identification and procedural guidance.
The Nevoscope is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The manufacturer operates from the United States.
Catalogue
Nevoscope Ref K954943
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nizar A. Mullani have in the registry?
The registry currently lists 1 device for Nizar A. Mullani. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nizar A. Mullani's devices?
Among its 1 most recently registered device, Nizar A. Mullani has devices listed in FDA 510(k) (1 device).
What risk classes do Nizar A. Mullani's devices fall under?
Among its 1 most recently registered device, the classes recorded for Nizar A. Mullani's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nizar A. Mullani in the registry?
The most recently registered devices listed for Nizar A. Mullani include NEVOSCOPE.