Philips Medizinsysteme Boeblingen GmbH, Cardiac AN - FDA 510(k) Clear...
25
Total
25
Cleared
0
Denied
Philips Medizinsysteme Boeblingen GmbH, Cardiac AN has 25 FDA 510(k) cleared cardiovascular devices. Based in Boeblingen, Baden-Wuerttemberg, DE.
Historical record: 25 cleared submissions from 2007 to 2014.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
25 devices
Cleared
May 19, 2014
INTELLIVUE PATIENT MONITOR MX400, INTELLIVUE PATIENT MONITOR MX450,...
Cardiovascular
28d
Cleared
Mar 26, 2014
INTELLIVUE CL RESPIRATION POD
Anesthesiology
244d
Cleared
Oct 17, 2013
INTELLIVUE PATIENT MONITOR MX500, INTELLIVUE PATIENT MONITOR MX550
Cardiovascular
115d
Cleared
Aug 16, 2013
INTELLIVUE PATIENT MONITOR
Cardiovascular
57d
Cleared
Jun 14, 2013
INTELLIVUE PATIENT MONITOR MX400
Cardiovascular
80d
Cleared
Jul 18, 2012
INTELLIVUE PATIENT MONITOR
Cardiovascular
163d
Cleared
Mar 22, 2012
PHYSIOLOGICAL MONITOR, PATIENT MONITOR
Cardiovascular
122d
Cleared
Oct 04, 2011
INTELLIVUE GUARDIAN SOFTWARE MODEL 866009, INTELLIVUE CL SP02 POD MODEL...
Cardiovascular
91d
Cleared
Sep 30, 2011
PHILIPS INTELLIVUE TCG10
Anesthesiology
224d
Cleared
Aug 17, 2011
PHILIPS AVALON FETAL/MATERNAL MONITORS FM20, FM30, FM40 AND FM50
Obstetrics & Gynecology
120d
Cleared
Mar 31, 2011
INTELLIVUE PATIENT MONITOR
Cardiovascular
28d
Cleared
Aug 31, 2010
INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216,...
Anesthesiology
84d