Philips Image Guided Therapy Corp

FDA Filings

This page includes the latest FDA filings for Philips Image Guided Therapy Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3016257349
FEI Number3016257349
NamePhilips Image Guided Therapy Corporation
Owner & OperatorPhilips Medical Systems International BV
Contact AddressTussendiepen 4
Drachten NL-NOTA 9206 AD NL
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address5905 Nathan Lane North
Plymouth, MN 55442 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
Philips Image Guided Therapy Corporation
VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter2020-09-02
Philips Image Guided Therapy Corporation
Reconnaissance PV .018 OTW Digital IVUS Catheter2020-05-22
Philips Image Guided Therapy Corporation [Philips Medical Systems International BV]
Stellarex Drug-Coated Angioplasty Balloon2018-11-26
Philips Image Guided Therapy Corporation [Philips Medical Systems International BV]
Stellarex 0.035? OTW Drug-coated Angioplasty Balloon2018-11-26

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