Covidien (Dba Medtronic) - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Covidien (Dba Medtronic) has 1 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Covidien (Dba Medtronic) Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Covidien (Dba Medtronic)
1 devices