Emergo Europe Consulting BV is one of 150 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Emergo Europe Consulting BV - FDA 510(k) Cleared Devices
Recent clearances: ICP TRIAGEMANAGER
1
Total
1
Cleared
0
Denied
Emergo Europe Consulting BV has 1 FDA 510(k) cleared medical devices. Based in Den Haag, NL.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Emergo Europe Consulting BV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Dekra Certification B.V as regulatory consultant.
FDA 510(k) Regulatory Record - Emergo Europe Consulting BV
1 devices