Hancock Medical, Inc.
Country not established
- Devices
- 1
What Hancock Medical, Inc. makes
Hancock Medical, Inc. makes the Beddr 200 System, a medical device used for sleep monitoring and respiratory assessment.
The Beddr 200 System is classified as a Class II device and is listed in the FDA 510(k) premarket notification database; the company is based in the United States.
Catalogue
Beddr 200 System Ref K190399
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hancock Medical, Inc. have in the registry?
The registry currently lists 1 device for Hancock Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hancock Medical, Inc.'s devices?
Among its 1 most recently registered device, Hancock Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hancock Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hancock Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hancock Medical, Inc. in the registry?
The most recently registered devices listed for Hancock Medical, Inc. include Beddr 200 System.