Medical Equipment Devices, Inc.
Country not established
- Devices
- 1
What Medical Equipment Devices, Inc. makes
Medical Equipment Devices, Inc. manufactures HEART-ALERT, a device designed for monitoring and alerting related to cardiac activity.
The company’s portfolio is regulated under Class I devices in the US and includes submissions via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Heart-Alert Ref K820444
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Equipment Devices, Inc. have in the registry?
The registry currently lists 1 device for Medical Equipment Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Equipment Devices, Inc.'s devices?
Among its 1 most recently registered device, Medical Equipment Devices, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Equipment Devices, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Equipment Devices, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medical Equipment Devices, Inc. in the registry?
The most recently registered devices listed for Medical Equipment Devices, Inc. include HEART-ALERT.