Philips Medical Systems, 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, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PCR ELEVA 1.2, PINNACLE3 SMARTARC, PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521
Philips Medical Systems, Inc. has 110 FDA 510(k) cleared radiology devices. Based in Mchenry, US.
Historical record: 110 cleared submissions from 1983 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., Entela, Inc. and Tuv Rheinland of North America, Inc..
FDA 510(k) Regulatory Record - Philips Medical Systems, Inc.
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