Advanced Respiratory
Country not established
- Devices
- 2
What Advanced Respiratory makes
Advanced Respiratory manufactures airway clearance systems designed to assist patients with respiratory conditions, including the ABI VEST and the Vest Airway Clearance System (Model 104). These devices use oscillating positive expiratory pressure (OPEP) technology to help mobilise and remove mucus from the lungs.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) clearance process. The devices are listed in the FDA’s 510(k) database. Advanced Respiratory operates from the United States.
Catalogue
Abi Vest Airway Clearance System Ref K012928
Regimes: 510(k) Registry: 510(k)The Vest Airway Clearance System, Model 104 Ref K024309
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Advanced Respiratory have in the registry?
The registry currently lists 2 devices for Advanced Respiratory. Devices recorded under merged duplicate company entries are counted once.
Which registries list Advanced Respiratory's devices?
Among its 2 most recently registered devices, Advanced Respiratory has devices listed in FDA 510(k) (2 devices).
What risk classes do Advanced Respiratory's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Advanced Respiratory's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Advanced Respiratory in the registry?
The most recently registered devices listed for Advanced Respiratory include ABI VEST AIRWAY CLEARANCE SYSTEM and THE VEST AIRWAY CLEARANCE SYSTEM, MODEL 104.