North American Grager
Country not established
- Devices
- 1
What North American Grager makes
North American Grager manufactures the DRAGER-VAPOR 19.1, a medical vaporizer designed for delivering precise anesthetic gases in surgical and procedural settings.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II device and is listed in the U.S. regulatory database.
Catalogue
Drager-Vapor 19.1 Ref K942055
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does North American Grager have in the registry?
The registry currently lists 1 device for North American Grager. Devices recorded under merged duplicate company entries are counted once.
Which registries list North American Grager's devices?
Among its 1 most recently registered device, North American Grager has devices listed in FDA 510(k) (1 device).
What risk classes do North American Grager's devices fall under?
Among its 1 most recently registered device, the classes recorded for North American Grager's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from North American Grager in the registry?
The most recently registered devices listed for North American Grager include DRAGER-VAPOR 19.1.