Philips Medizin Systeme Boblingen GmbH - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Philips Medizin Systeme Boblingen GmbH has 12 FDA 510(k) cleared cardiovascular devices. Based in Andover, US.
Historical record: 12 cleared submissions from 2001 to 2015.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
12 devices
Cleared
Oct 21, 2015
Philips IntelliVue GuardianSoftware
Cardiovascular
117d
Cleared
Nov 25, 2014
PHILIPS AVALON FETAL / MATERNAL MONITORS FM20, FM30, FM40 AND FM50
Obstetrics & Gynecology
266d
Cleared
Mar 22, 2012
INTELLIVUE PATIENT MONITOR
Cardiovascular
101d
Cleared
Mar 18, 2011
PHILIPS AVALON FETAL MONITOR
Obstetrics & Gynecology
165d
Cleared
Oct 21, 2010
INTELLIVUE PATIENT MONITOR, MODELS MP2, X2, MP5, MP5T, MP20, MP30, MP40,...
Cardiovascular
44d
Cleared
May 04, 2009
PHILIPS M3001A MULTI MEASUREMENT SERVER
Anesthesiology
81d
Cleared
Nov 24, 2008
PHILIPS INTELLIVUE MP5 PATIENT MONITOR
Cardiovascular
21d
Cleared
Mar 24, 2006
THE PHILIPS MP20,MP30,MP40,MP50,MP60,MP70,MP80 AND MP90 INTELLIVUE ATIENT...
Cardiovascular
23d
Cleared
Nov 12, 2004
THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, AND MP90 INTELLIVUE PATIENT...
Cardiovascular
28d
Cleared
Oct 10, 2003
THE PHILIPS INTELLIVUE MP40, MP50, MP60, MP70,AND MP90 PATIENT MONITORS,...
Cardiovascular
28d
Cleared
May 29, 2003
THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20
Cardiovascular
17d
Cleared
Dec 03, 2001
MODIFICATION TO AGILENT COMPONENT MONITORING SYSTEM (CMS), V24/V26 PATIENT...
Cardiovascular
28d