Medata, Inc.
Country not established
- Devices
- 1
What Medata, Inc. makes
Medata, Inc. manufactures HEARTPRINT, a diagnostic device used for cardiac assessment, likely involving electrophysiological data analysis or arrhythmia detection.
The company’s portfolio is regulated under FDA’s Class II device classification, with devices authorised via the 510(k) pathway. It operates from the United States.
Catalogue
Heartprint Ref K942862
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medata, Inc. have in the registry?
The registry currently lists 1 device for Medata, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medata, Inc.'s devices?
Among its 1 most recently registered device, Medata, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medata, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medata, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medata, Inc. in the registry?
The most recently registered devices listed for Medata, Inc. include HEARTPRINT.