Medical Device Manufacturer · US , Mansfield , MA

Covidien LP - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2009

Total

Cleared

Denied

Covidien LP has 3 FDA 510(k) cleared medical devices. Based in Mansfield, US.

Historical record: 3 cleared submissions from 2009 to 2016.

Browse the FDA 510(k) cleared devices submitted by Covidien LP Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Covidien LP

3 devices

1-3 of 3