Kestra Medical Technologies receives FDA premarket approval for ASSURE wearable cardioverter defibrillator

Kestra Medical Technologies

3 August 2021 - Kestra Medical Technologies announced today that the company has received U.S. FDA premarket approval for the ASSURE wearable cardioverter defibrillator system.

The ASSURE wearable cardioverter defibrillator system represents the next generation of monitoring and therapy to protect patients at risk of sudden cardiac death.

Read Kestra Medical Technologies press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Outcome , US , Device