Cardiosense, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiosense, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CardioTag™
2
Total
1
Cleared
1
Denied
Cardiosense, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.
Latest FDA clearance: Jul 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiosense, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiosense, Inc.
2 devices