Personal Emergency Response System
Country not established
- Devices
- 1
What Personal Emergency Response System makes
The company manufactures medical alert systems, including wearable devices like the Model 2200 and 4400 V/T, designed for emergency response in home or public settings. These systems enable users to call for assistance via a voice or vibration alert, connecting them to emergency services or designated contacts.
The portfolio consists of Class II medical devices, regulated under the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry and are intended for use in the United States.
Catalogue
Medical Alert System, Model 2200 & 4400 V/T Ref K904796
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Personal Emergency Response System have in the registry?
The registry currently lists 1 device for Personal Emergency Response System. Devices recorded under merged duplicate company entries are counted once.
Which registries list Personal Emergency Response System's devices?
Among its 1 most recently registered device, Personal Emergency Response System has devices listed in FDA 510(k) (1 device).
What risk classes do Personal Emergency Response System's devices fall under?
Among its 1 most recently registered device, the classes recorded for Personal Emergency Response System's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Personal Emergency Response System in the registry?
The most recently registered devices listed for Personal Emergency Response System include MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T.