FDA 510(k) Applications Submitted by HAUKE SCHIK

FDA 510(k) Number Submission Date Device Name Applicant
K050141 01/25/2005 THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70 AND MP90 INTELLIVUE PATIENT MONITORS PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH
K040304 02/09/2004 PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50 PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH
K061052 04/17/2006 THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90 PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
K051106 05/02/2005 THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, MP80 AND MP90 INTELLIVUE PATIENT MONITORS PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH
K031481 05/12/2003 THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20 PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH
K061610 06/09/2006 PHILIPS MODEL MP20, MP30, MP40, MP50, MP60, MP70, MP80 AND MP90 INTELLIVUE PATIENT MONITORS PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH
K032858 09/12/2003 THE PHILIPS INTELLIVUE MP40, MP50, MP60, MP70,AND MP90 PATIENT MONITORS, RELEASE B.O. PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH
K052801 10/03/2005 INTELLIVUE PATIENT MONITORS WITH RELEASE C.02, MODELS MP20, MP30, MP40, MP50, MP60, MP70, MP80 AND MP90 PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH


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