La Societe Fianciere Senefin
Country not established
- Devices
- 1
What La Societe Fianciere Senefin makes
La Societe Fianciere Senefin manufactures the Brook Life Saving Airway Device, a Class I medical device designed for emergency airway management.
The Brook Life Saving Airway Device is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Brook Life Saving Airway Device #900 & Ref K832435
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does La Societe Fianciere Senefin have in the registry?
The registry currently lists 1 device for La Societe Fianciere Senefin. Devices recorded under merged duplicate company entries are counted once.
Which registries list La Societe Fianciere Senefin's devices?
Among its 1 most recently registered device, La Societe Fianciere Senefin has devices listed in FDA 510(k) (1 device).
What risk classes do La Societe Fianciere Senefin's devices fall under?
Among its 1 most recently registered device, the classes recorded for La Societe Fianciere Senefin's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from La Societe Fianciere Senefin in the registry?
The most recently registered devices listed for La Societe Fianciere Senefin include BROOK LIFE SAVING AIRWAY DEVICE #900 &.