Hawkins Intl.
Country not established
- Devices
- 1
What Hawkins Intl. makes
Hawkins Intl. manufactures the ULTIMATE-AIRE, a medical device designed for respiratory support or air filtration in clinical settings.
The ULTIMATE-AIRE is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Ultimate-Aire Ref K813258
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hawkins Intl. have in the registry?
The registry currently lists 1 device for Hawkins Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hawkins Intl.'s devices?
Among its 1 most recently registered device, Hawkins Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Hawkins Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hawkins Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hawkins Intl. in the registry?
The most recently registered devices listed for Hawkins Intl. include ULTIMATE-AIRE.