Anesco
Country not established
- Devices
- 1
What Anesco makes
Anesco manufactures the AES (Anesco Evacuation System), an active waste anesthetic gas evacuation system designed to capture and remove anesthetic gases from the operating room environment.
The AES is classified as a Class II medical device and is listed in the FDA 510(k) database. Anesco is based in the United States. The record supports this information.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anesco have in the registry?
The registry currently lists 1 device for Anesco. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anesco's devices?
Among its 1 most recently registered device, Anesco has devices listed in FDA 510(k) (1 device).
What risk classes do Anesco's devices fall under?
Among its 1 most recently registered device, the classes recorded for Anesco's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anesco in the registry?
The most recently registered devices listed for Anesco include AES, (ANESCO EVACUATION SYSTEM) ACTIVE WASTE ANESTHETIC GAS EVACUATION SYSTEM.