Promega Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Promega Corporation - FDA 510(k) Cleared Devices
Recent clearances: OncoMate MSI Dx Analysis System
1
Total
1
Cleared
0
Denied
Promega Corporation has 1 FDA 510(k) cleared medical devices. Based in Madison, US.
Last cleared in 2021. Active since 2021. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Promega Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Promega Corporation
1 devices