Midmark Diagnostics Group is one of 22702 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Midmark Diagnostics Group - FDA 510(k) Cleared Devices
Recent clearances: MIDMARK DIAGNOSTICS IQMARK VITAL SIGNS MONITOR
1
Total
1
Cleared
0
Denied
Midmark Diagnostics Group has 1 FDA 510(k) cleared medical devices. Based in Torrance, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Midmark Diagnostics Group Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Midmark Diagnostics Group
1 devices