Medical Device Manufacturer · US , Shelton , CT

Philips Medical Systems North America Co. - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 2001

Total

Cleared

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) Regulatory Record - Philips Medical Systems North America Co.

24 devices

1-24 of 24

WIRELESS PORTABLE DETECTOR FD-W17

K090625 · MQB

Radiology · 15d

Cleared Mar 16, 2009

VERADIUS, MODEL 718-130

K090590 · OWB

Radiology · 12d

Cleared Oct 08, 2008

SURESIGNS VS2 VITAL SIGNS MONITOR, SURESIGNS VM1 PATIENT MONITOR, SURESIGNS...

K082280 · MHX

Cardiovascular · 58d

Cleared Jan 05, 2007

PHILIPS XD-S DIRECT RADIOGRAPHY WORKSTATION/PACKAGE

K063781 · LLZ

Radiology · 15d

Cleared Oct 18, 2006

MASIMO SET SPO2 MODULE FOR PHILIPS AND M3001A MULTI-MEASUREMENT SERVER OPTION...

ALLURA 3D-CA, RELEASE 1

INTEGRIS 3D-RA, RELEASE 4.2

K040254 · LLZ

Radiology · 15d

Cleared Aug 14, 2003

PHILIPS FRESCO RELEASE 1

K031836 · LLZ

Radiology · 62d

Cleared Jul 21, 2003

DUNLEE FORMAT COLLIMATOR FAMILY

K031597 · IZW

Radiology · 61d

Cleared Jun 17, 2003

PHILIPS EASYDIAGNOST ELEVA

PHILIPS EASYVISION WORKSTATION RELEASE 6

K023137 · LLZ

Radiology · 90d

Cleared Nov 22, 2002

PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.0

K022899 · JAA

Radiology · 80d

Cleared Oct 25, 2002

PHILIPS HARMONY RELEASE 1

Philips Medical Systems North America Co. - FDA 510(k) Cleared Devices

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