Rest Technologies, Inc.
Country not established
- Devices
- 1
What Rest Technologies, Inc. makes
Rest Technologies, Inc. manufactures the DREAM CATCHER, a medical device designed for use in sleep monitoring or respiratory support applications.
The DREAM CATCHER is classified as a Class II device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Dream Catcher Ref K972122
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rest Technologies, Inc. have in the registry?
The registry currently lists 1 device for Rest Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rest Technologies, Inc.'s devices?
Among its 1 most recently registered device, Rest Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rest Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rest Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rest Technologies, Inc. in the registry?
The most recently registered devices listed for Rest Technologies, Inc. include DREAM CATCHER.