American Anesthesia, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What American Anesthesia, Inc. makes
American Anesthesia, Inc. manufactures anesthesia machines, including the PHOENIX, PHOENIX-C, and related variants, designed for administering controlled gases and vapors during surgical procedures.
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
Phoenix Anesthesia Machine Ref K853139
Regimes: 510(k) Registry: 510(k)Phoenix-C Anesthesia Machine Ref K864644
Regimes: 510(k) Registry: 510(k)Phoenix Anesthesia Machine Ref K844563
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Anesthesia, Inc. have in the registry?
The registry currently lists 3 devices for American Anesthesia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Anesthesia, Inc.'s devices?
Among its 3 most recently registered devices, American Anesthesia, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do American Anesthesia, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for American Anesthesia, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Anesthesia, Inc. in the registry?
The most recently registered devices listed for American Anesthesia, Inc. include PHOENIX ANESTHESIA MACHINE and PHOENIX-C ANESTHESIA MACHINE.