Philips Medical Systems North America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Medical Systems North America, Inc. - FDA 510(k) Cleared Devi...
Recent clearances: ALLURA XPER OR TABLE SERIES, HEARTSTART MRX MONITOR/DEFIBRILLATOR, THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90 INTELLIVUE PATIENT MONITORS
71
Total
71
Cleared
0
Denied
Philips Medical Systems North America, Inc. has 71 FDA 510(k) cleared radiology devices. Based in Shelton, US.
Historical record: 71 cleared submissions from 1989 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.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Philips Medical Systems North America, Inc.
71 devices
Cleared
Aug 09, 2010
ALLURA XPER OR TABLE SERIES
Radiology
25d
Cleared
Nov 22, 2006
HEARTSTART MRX MONITOR/DEFIBRILLATOR
Cardiovascular
112d
Cleared
Sep 20, 2006
THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90 INTELLIVUE PATIENT...
Cardiovascular
44d
Cleared
May 26, 2006
THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS...
Cardiovascular
39d
Cleared
Feb 09, 2005
MULTIDIAGNOST ELEVA
Radiology
16d
Cleared
Nov 02, 2004
PHILIPS ORTHOPAEDIC APPLICATIONS
Radiology
15d
Cleared
Jul 26, 2004
PANORAMA 1.0T
Radiology
42d
Cleared
Dec 09, 2003
ALLURA XPER FD20
Radiology
11d
Cleared
May 13, 2003
PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.2
Radiology
15d
Cleared
Jan 18, 2002
TANSMIT/RECEIVE QUADRATURE BODY COIL 3.0T
Radiology
56d
Cleared
Jan 22, 2001
PHILIPS EASY VISION FAMILY WORKSTATION OPTION MR QUANTITATIVE FLOW
Radiology
76d
Cleared
Dec 27, 2000
GYROSCAN INTERA 3.0T
Radiology
43d
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