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SpO2 patient monitoring system
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Covidien's Nellcor Pulse Oximeters Has Obtained 510(K) Clearance with Labeling From US FDA
May 29, 2013Patient monitoring and respiratory care devices provider Covidien's Nellcor Pulse Oximeters has obtained 510(k) clearance with labeling from US Food and Drug Administration (FDA). Nellcor Pulse Oximeters facilitates in noninvasive ...
Tags: Covidien's Nellcor, Medicine
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The Nellcor Pulse Oximetry Portfolio, Which Is Used to Measure Arterial Oxygen Saturation
May 23, 2013Covidien has announced that its Nellcor pulse oximetry portfolio received the US Food and Drug Administration (FDA) 510(k) clearance for motion claims. The Nellcor pulse oximetry portfolio, which is used to measure arterial oxygen ...
Tags: Covidien, Motion Claims
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Nellcor Bedside SpO2 Patient Monitoring System Is Introduced by Covidien
Dec 19, 2012Covidien will introduce its Nellcor Bedside SpO2 Patient Monitoring system at the European Society of Anesthesiology Congress held between 9-12 June 2012 in Paris, France. The Nellcor system utilizes OxiMax technology for monitoring ...
Tags: European Society of Anesthesiology Congress, Patient Monitoring system
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FDA Has Granted Clearance to Covidien's Nellcor Bedside SpO2 Patient Monitoring System
Dec 17, 2012The US Food and Drug Administration (FDA) has granted 510(k) clearance to Covidien's Nellcor bedside SpO2 patient monitoring system. The Nellcor bedside SpO2 monitor, which utilizes OxiMax technology, is designed for detecting heart rate ...
Tags: FDA, clearance, Nellcor, SpO2 patient monitoring system, SpO2 monitor
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