Mgc Diagnostics Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mgc Diagnostics Corporation - FDA 510(k) Cleared Devices
Recent clearances: Fenom Flo™ FeNO Monitoring System
1
Total
1
Cleared
0
Denied
Mgc Diagnostics Corporation has 1 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Latest FDA clearance: Nov 2025. Active since 2025. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Mgc Diagnostics Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pathmaker FDA Law, PLLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mgc Diagnostics Corporation
1 devices