Kestra Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kestra Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ASSURE Wearable ECG
1
Total
1
Cleared
0
Denied
Kestra Medical Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Kirkland, US.
Latest FDA clearance: May 2024. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Kestra Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kestra Medical Technologies, Inc.
1 devices