Respiri Limited
AustraliaFDA applicant, unverified
- Devices
- 1
What Respiri Limited makes
Respiri Limited makes the wheezo WheezeRate Detector, a device designed to detect and measure wheezing in patients.
The wheezo WheezeRate Detector is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
wheezo WheezeRate Detector Ref K202062
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Respiri Limited have in the registry?
The registry currently lists 1 device for Respiri Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Respiri Limited's devices?
Among its 1 most recently registered device, Respiri Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Respiri Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Respiri Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Respiri Limited in the registry?
The most recently registered devices listed for Respiri Limited include wheezo WheezeRate Detector.