Nevap, Inc.
Country not established
- Devices
- 1
What Nevap, Inc. makes
Nevap, Inc. manufactures the NeVap Aspire Subglottic Suction Endotracheal Tube (ASSET), a device designed for airway management in critical care settings. It includes a built-in suction channel and a preloaded stylet to facilitate placement and reduce complications during intubation.
The NeVap Aspire Subglottic Suction Endotracheal Tube (ASSET) is classified as a Class II medical device under FDA regulations and has undergone 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nevap, Inc. have in the registry?
The registry currently lists 1 device for Nevap, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nevap, Inc.'s devices?
Among its 1 most recently registered device, Nevap, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nevap, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nevap, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nevap, Inc. in the registry?
The most recently registered devices listed for Nevap, Inc. include NeVap Aspire Subglottic Suction Endotracheal Tube (ASSET) with Preloaded Stylet.