Philips Medical Systems North America Co. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Philips Medical Systems North America Co. has 24 FDA 510(k) cleared radiology devices. Based in Shelton, US.
Historical record: 24 cleared submissions from 2001 to 2010.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Philips Medical Systems North America...
24 devices
Cleared
Sep 30, 2010
EP NAVIGATOR R3
Radiology
142d
Cleared
Mar 24, 2009
WIRELESS PORTABLE DETECTOR FD-W17
Radiology
15d
Cleared
Mar 16, 2009
VERADIUS, MODEL 718-130
Radiology
12d
Cleared
Oct 08, 2008
SURESIGNS VS2 VITAL SIGNS MONITOR, SURESIGNS VM1 PATIENT MONITOR, SURESIGNS...
Cardiovascular
58d
Cleared
Jan 05, 2007
PHILIPS XD-S DIRECT RADIOGRAPHY WORKSTATION/PACKAGE
Radiology
15d
Cleared
Oct 18, 2006
MASIMO SET SPO2 MODULE FOR PHILIPS AND M3001A MULTI-MEASUREMENT SERVER OPTION...
Anesthesiology
72d
Cleared
Sep 15, 2006
PULSERA
Radiology
92d
Cleared
Sep 06, 2006
XCELERA
Radiology
54d
Cleared
Apr 04, 2006
XPERCT
Radiology
15d
Cleared
Apr 08, 2005
FLXIS
Radiology
22d
Cleared
Feb 15, 2005
ACHIEVA FAMILY
Radiology
92d
Cleared
Oct 04, 2004
PRACTIX CONVENIO
Radiology
34d