Cardea Associates, Inc. is one of 19346 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardea Associates, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CARDEASCREEN
1
Total
1
Cleared
0
Denied
Cardea Associates, Inc. has 1 FDA 510(k) cleared medical devices. Based in Woodinville, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardea Associates, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cardea Associates, Inc.
1 devices