Heartforce Medical, Inc.
Country not established
- Devices
- 1
What Heartforce Medical, Inc. makes
Heartforce Medical, Inc. manufactures the Digital Ballistocardiograph (Model DGB 300), a device used to measure and analyze ballistocardiographic waveforms for cardiac assessment.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Digital Ballistocardiograph, Model Dgb 300 Ref K081603
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Heartforce Medical, Inc. have in the registry?
The registry currently lists 1 device for Heartforce Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Heartforce Medical, Inc.'s devices?
Among its 1 most recently registered device, Heartforce Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Heartforce Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Heartforce Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Heartforce Medical, Inc. in the registry?
The most recently registered devices listed for Heartforce Medical, Inc. include DIGITAL BALLISTOCARDIOGRAPH, MODEL DGB 300.