Creagh Medical is one of 89 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Creagh Medical - FDA 510(k) Cleared Devices
Recent clearances: 014 Hydrophilic Coated PTA Balloon Dilatation Catheter
1
Total
1
Cleared
0
Denied
Creagh Medical has 1 FDA 510(k) cleared medical devices. Based in Ballinasloe, IE.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Creagh Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Surmodics as regulatory consultant.
FDA 510(k) Regulatory Record - Creagh Medical
1 devices