ASSURE Wearable ECG
May 2024
153d
Kestra Medical Technologies, Inc.
1
Total
1
Cleared
0
Denied
Kestra Medical Technologies, Inc. — FDA 510(k) Submissions
Kestra Medical Technologies, Inc. has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electrocardiograph, Ambulatory (without Analysis) . Use the specialty filter in the sidebar to narrow results.
1 devices