Philips Medizin Systeme Boblingen GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K151736Philips IntelliVue GuardianSoftwareOctober 21, 2015
K140535PHILIPS AVALON FETAL / MATERNAL MONITORS FM20, FM30, FM40 AND FM50November 25, 2014
K113657INTELLIVUE PATIENT MONITORMarch 22, 2012
K102958PHILIPS AVALON FETAL MONITORMarch 18, 2011
K102562INTELLIVUE PATIENT MONITOR, MODELS MP2, X2, MP5, MP5T, MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP9October 21, 2010
K090360PHILIPS M3001A MULTI MEASUREMENT SERVERMay 4, 2009
K083228PHILIPS INTELLIVUE MP5 PATIENT MONITORNovember 24, 2008
K060541THE PHILIPS MP20,MP30,MP40,MP50,MP60,MP70,MP80 AND MP90 INTELLIVUE ATIENT MONITORSMarch 24, 2006
K042845THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, AND MP90 INTELLIVUE PATIENT MONITORSNovember 12, 2004
K032858THE PHILIPS INTELLIVUE MP40, MP50, MP60, MP70,AND MP90 PATIENT MONITORS, RELEASE B.O.October 10, 2003
K031481THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20May 29, 2003
K013624MODIFICATION TO AGILENT COMPONENT MONITORING SYSTEM (CMS), V24/V26 PATIENT MONITORS, BLOOD ANALYSIS December 3, 2001