Mc3, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mc3, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Nautilus VF ECMO Oxygenator, MC3 Crescent Jugular Dual Lumen Catheter
2
Total
2
Cleared
0
Denied
Mc3, Inc. has 2 FDA 510(k) cleared medical devices. Based in Dexter, US.
Last cleared in 2023. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mc3, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mc3, Inc.
2 devices