Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) - FDA 510(...
Recent clearances: EverCrossTM 0.035 OTW PTA Dilatation Catheter
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) Regulatory Record - Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.)
1 devices