Medical Device Manufacturer · US , Mansfield , MA

Covidien (Dba Medtronic) - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Total

Cleared

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.

Covidien (Dba Medtronic) is one of 4719 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Covidien (Dba Medtronic)

1 devices

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