Cardiocom is one of 25405 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Cardiocom has 1 FDA 510(k) cleared medical devices. Based in Minneapolis,, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiocom 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 - Cardiocom
1 devices