Curatia Medical is one of 19001 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curatia Medical - FDA 510(k) Cleared Devices
Recent clearances: Vela RX PTA Balloon Dilatation Catheter
1
Total
1
Cleared
0
Denied
Curatia Medical has 1 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Curatia Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jcq Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Curatia Medical
1 devices