Anesthesia Assoc., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Anesthesia Assoc., Inc. makes
Anesthesia Assoc., Inc. manufactures a universal control arm, a nerve stimulator model AA 1050, and a jet ventilator/jetting device for use in anesthesia and respiratory support.
These devices are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Universal Control Arm Ref K833871
Regimes: 510(k) Registry: 510(k)Nerve Stimulator Model Aa 1050 Ref K811614
Regimes: 510(k) Registry: 510(k)Jet Ventilator/Jetting Device Ref K921926
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anesthesia Assoc., Inc. have in the registry?
The registry currently lists 3 devices for Anesthesia Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anesthesia Assoc., Inc.'s devices?
Among its 3 most recently registered devices, Anesthesia Assoc., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Anesthesia Assoc., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Anesthesia Assoc., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anesthesia Assoc., Inc. in the registry?
The most recently registered devices listed for Anesthesia Assoc., Inc. include UNIVERSAL CONTROL ARM, NERVE STIMULATOR MODEL AA 1050 and JET VENTILATOR/JETTING DEVICE.