Mc3 Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mc3 Incorporated - FDA 510(k) Cleared Devices
Recent clearances: Nautilus Smart ECMO Module, MC3 Vascular Access Kit 21030, MC3 Jugular Dual Lumen Catheter
4
Total
4
Cleared
0
Denied
Mc3 Incorporated has 4 FDA 510(k) cleared medical devices. Based in Dexter, US.
Historical record: 4 cleared submissions from 2017 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mc3 Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mc3 Incorporated
4 devices