Dri-Aire, Inc.
Country not established
- Devices
- 1
What Dri-Aire, Inc. makes
Dri-Aire, Inc. manufactures compressed air and oxygen generation and delivery systems designed for medical and industrial applications, ensuring controlled gas supply for patient care or operational use.
These systems are classified as Class II devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Compressed Air & Oxygen Gen./Delivery Sy Ref K803232
510(k) 510(k)
Frequently asked questions
How many devices does Dri-Aire, Inc. have in the registry?
The registry currently lists 1 device for Dri-Aire, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dri-Aire, Inc.'s devices?
Among its 1 most recently registered device, Dri-Aire, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dri-Aire, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dri-Aire, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dri-Aire, Inc. in the registry?
The most recently registered devices listed for Dri-Aire, Inc. include COMPRESSED AIR & OXYGEN GEN./DELIVERY SY.