Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) - FDA 510(...
1
Total
1
Cleared
0
Denied
Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) has 1 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medtronic, Inc. (Formerly D.B.A. Ev3,...
1 devices