Humana USA, Inc.
Country not established
- Devices
- 1
What Humana USA, Inc. makes
Humana USA, Inc. manufactures the DIGICAP, a device designed for capturing and managing digital health data, likely for remote patient monitoring or telehealth applications.
The DIGICAP is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Digicap Ref K012199
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Humana USA, Inc. have in the registry?
The registry currently lists 1 device for Humana USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Humana USA, Inc.'s devices?
Among its 1 most recently registered device, Humana USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Humana USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Humana USA, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Humana USA, Inc. in the registry?
The most recently registered devices listed for Humana USA, Inc. include DIGICAP.