Foregger
Country not established
- Devices
- 2
What Foregger makes
Foregger manufactures anesthesia machines and I.P.P.B. manifold/nebulizer circuits, which are used in surgical and procedural settings to deliver controlled breathing gases and aerosolized medications to patients.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Anesthesia Machine Ref K771057
Regimes: 510(k) Registry: 510(k)I.P.P.B. Manifold/Nebulizer (Circuit) Ref K760263
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Foregger have in the registry?
The registry currently lists 2 devices for Foregger. Devices recorded under merged duplicate company entries are counted once.
Which registries list Foregger's devices?
Among its 2 most recently registered devices, Foregger has devices listed in FDA 510(k) (2 devices).
What risk classes do Foregger's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Foregger's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Foregger in the registry?
The most recently registered devices listed for Foregger include ANESTHESIA MACHINE and I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT).