Cardiomedix, Inc. is one of 18486 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiomedix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ECG SENTINEL System
1
Total
1
Cleared
0
Denied
Cardiomedix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Evanston, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiomedix, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cardiomedix, Inc.
1 devices