Mdoloris Medical Systems Sas is one of 285 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Mdoloris Medical Systems Sas - FDA 510(k) Cleared Devices
Recent clearances: ANI Monitor
1
Total
1
Cleared
0
Denied
Mdoloris Medical Systems Sas has 1 FDA 510(k) cleared medical devices. Based in Lille, FR.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mdoloris Medical Systems Sas Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Speed TO Market, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Mdoloris Medical Systems Sas
1 devices