Medical Device Manufacturer · US , Boulder , CO

Covidien, Formerly Valleylab, - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2011

Total

Cleared

Denied

Covidien, Formerly Valleylab, has 1 FDA 510(k) cleared medical devices. Based in Boulder, US.

Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Covidien, Formerly Valleylab,

1 devices

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