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.

Philips Medical Systems North America Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Philips Medical Systems North America Co.

24 devices

1-12 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...

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

FDA 510(k) Regulatory Record - Philips Medical Systems North America Co.

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