FDA 510(k), K141518, Nellcor Bedside Respiratory Patient Monitoring System
FDA 510(k), K141518, Nellcor Bedside Respiratory Patient Monitoring System
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$149.00 USD
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$149.00 USD
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510(K) Number: K141518
Device Name: Nellcor Bedside Respiratory Patient Monitoring System
Manufacturer: COVIDIEN
Device Classification Name: oximeter
Regulation Number: 870.2700
Classification Product Code: DQA
Date Received: 06/09/2014
Decision Date: 03/05/2015
Regulation Medical Specialty: Cardiovascular
Device Name: Nellcor Bedside Respiratory Patient Monitoring System
Manufacturer: COVIDIEN
Device Classification Name: oximeter
Regulation Number: 870.2700
Classification Product Code: DQA
Date Received: 06/09/2014
Decision Date: 03/05/2015
Regulation Medical Specialty: Cardiovascular