Heart Alert, Inc.
Country not established
- Devices
- 1
What Heart Alert, Inc. makes
Heart Alert, Inc. makes the P.H.D. - Personal Heart Device Model 5258, a personal heart monitoring device.
This device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
P.H.D. - Personal Heart Device Model 5258 Ref K963904
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Heart Alert, Inc. have in the registry?
The registry currently lists 1 device for Heart Alert, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Heart Alert, Inc.'s devices?
Among its 1 most recently registered device, Heart Alert, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Heart Alert, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Heart Alert, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Heart Alert, Inc. in the registry?
The most recently registered devices listed for Heart Alert, Inc. include P.H.D. - PERSONAL HEART DEVICE MODEL 5258.