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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 28 Results
ProductCode: IYN Applicant: PHILIPS ULTRASOUND, INC Decision Date To: 08/29/2016
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epiq 5 diagnostic ultrasound system; epiq 7 diagnostic ultrasound system; affiniti 50 diagnostic ultrasound system; affiniti 70 diagnostic ultrasound system Philips Ultrasound, Inc. K163120 01/10/2017
epiq diagnostic ultrasound system PHILIPS ULTRASOUND, INC. K132304 08/21/2013
epiq diagnostic ultrasound system Philips Ultrasound, Inc. K200304 03/06/2020
epiq diagnostic ultrasound system series, affiniti diagnostic ultrasound system series, cx50 diagnostic ultrasound system, sparq diagnostic ultrasound system, lumify diagnostic ultrasound system Philips Ultrasound, Inc. K201012 05/01/2020
epiq diagnostic ultrasound system, epiq 5 diagnostic ultrasound system, epiq 7 diagnostic ultrasound system, affiniti 30 diagnostic ultrasound system, affiniti 50 diagnostic ultrasound system, affiniti 70 diagnostic ultrasound system Philips Ultrasound, Inc. K182857 11/09/2018
epiq series diagnostic ultrasound systems Philips Ultrasound, Inc. K202216 09/02/2020
hd11 diagnostic ultrasound system PHILIPS ULTRASOUND, INC. K043535 01/06/2005
hd11 diagnostic ultrasound system PHILIPS ULTRASOUND, INC. K062247 08/18/2006
hd15 diagnostic ultrasound system PHILIPS ULTRASOUND, INC. K081661 06/24/2008
hdi 5000 diagnostic ultrasound system PHILIPS ULTRASOUND, INC. K034003 01/08/2004
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