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FDA 510(k), K101600, INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216, INTELLIVUE PATIENT MONITORS MP5, MP2, X2 MODEL
FDA 510(k), K101600, INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216, INTELLIVUE PATIENT MONITORS MP5, MP2, X2 MODEL
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510(K) Number: K101600
Device Name: INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216, INTELLIVUE PATIENT MONITORS MP5, MP2, X2 MODEL
Manufacturer: PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH, CARDIAC AN
Device Classification Name: Oximeter
Regulation Number: 870.2700
Classification Product Code: DQA
Date Received: 06/08/2010
Decision Date: 08/31/2010
Regulation Medical Specialty: Cardiovascular
Device Name: INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216, INTELLIVUE PATIENT MONITORS MP5, MP2, X2 MODEL
Manufacturer: PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH, CARDIAC AN
Device Classification Name: Oximeter
Regulation Number: 870.2700
Classification Product Code: DQA
Date Received: 06/08/2010
Decision Date: 08/31/2010
Regulation Medical Specialty: Cardiovascular
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