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» Covidien Announces FDA 510(k) Clearance and CE Mark for Nellcor™ Bedside Respiratory Patient Monitoring System
Covidien Announces FDA 510(k) Clearance and CE Mark for Nellcor™ Bedside Respiratory Patient Monitoring System
Covidien Announces FDA 510(k) Clearance and CE Mark for Nellcor™ Bedside Respiratory Patient Monitoring System
Submitted by
moderatorj
on October 4, 2012 - 10:42pm
Source:
Yahoo/BusinessWire
News Tags:
Covidien
FDA
CE Mark
monitoring
Respiratory
Headline:
Covidien Announces FDA 510(k) Clearance and CE Mark for Nellcor™ Bedside Respiratory Patient Monitoring System
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