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Home > Newsletters > FDAnews Device Daily Bulletin > Covidien Patient Monitoring System Receives Clearance

FDAnews Device Daily Bulletin

Oct. 11, 2012 | Vol. 9 No. 200

Covidien Patient Monitoring System Receives Clearance

Covidien has received FDAO 510(k) clearance and CE Mark approval for its Nellcor bedside respiratory patient monitoring system.
Clinical Innovation + Technology

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