Coactiv, LLC is one of 25165 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Coactiv, LLC has 1 FDA 510(k) cleared medical devices. Based in Denton, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Coactiv, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Coactiv, LLC
1 devices