Ecordum, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ecordum, Inc. - FDA 510(k) Cleared Devices
Recent clearances: eCordum Cardiac Monitor (eCordum CM)
1
Total
1
Cleared
0
Denied
Ecordum, Inc. has 1 FDA 510(k) cleared medical devices. Based in East Northport, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ecordum, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Biologics Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Ecordum, Inc.
1 devices