Elastic Care Incorporated
CanadaFDA applicant, unverified
- Devices
- 1
What Elastic Care Incorporated makes
Elastic Care Incorporated manufactures the LifePath Remote Patient Monitoring Platform, a digital solution designed to track and transmit patient health data remotely for continuous clinical oversight.
The platform is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
LifePath Remote Patient Monitoring Platform Ref K211822
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elastic Care Incorporated have in the registry?
The registry currently lists 1 device for Elastic Care Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elastic Care Incorporated's devices?
Among its 1 most recently registered device, Elastic Care Incorporated has devices listed in FDA 510(k) (1 device).
What risk classes do Elastic Care Incorporated's devices fall under?
Among its 1 most recently registered device, the classes recorded for Elastic Care Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elastic Care Incorporated in the registry?
The most recently registered devices listed for Elastic Care Incorporated include LifePath Remote Patient Monitoring Platform.