Eugene Scarberry
Country not established
- Devices
- 1
What Eugene Scarberry makes
Eugene Scarberry manufactures the DIXIE USA PTL, a pharyngeal tracheal lumen designed for airway management in medical procedures.
The pharyngeal tracheal lumen is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Dixie Usa Ptl, Pharyngeal Tracheal Lumen Ref K831481
510(k) 510(k)
Frequently asked questions
How many devices does Eugene Scarberry have in the registry?
The registry currently lists 1 device for Eugene Scarberry. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eugene Scarberry's devices?
Among its 1 most recently registered device, Eugene Scarberry has devices listed in FDA 510(k) (1 device).
What risk classes do Eugene Scarberry's devices fall under?
Among its 1 most recently registered device, the classes recorded for Eugene Scarberry's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eugene Scarberry in the registry?
The most recently registered devices listed for Eugene Scarberry include DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN.