Resapp Health
AustraliaFDA applicant, unverified
- Devices
- 1
What Resapp Health makes
Resapp Health manufactures SleepCheckRx, a diagnostic device designed to assess sleep patterns and provide clinical insights for patient evaluation.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. Resapp Health operates from the United States.
Catalogue
SleepCheckRx Ref K213360
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Resapp Health have in the registry?
The registry currently lists 1 device for Resapp Health. Devices recorded under merged duplicate company entries are counted once.
Which registries list Resapp Health's devices?
Among its 1 most recently registered device, Resapp Health has devices listed in FDA 510(k) (1 device).
What risk classes do Resapp Health's devices fall under?
Among its 1 most recently registered device, the classes recorded for Resapp Health's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Resapp Health in the registry?
The most recently registered devices listed for Resapp Health include SleepCheckRx.