Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
1 to 8 of 8 Results
ProductCode: ITX Applicant: PHILIPS HEALTHCARE Decision Date To: 05/15/2024
Results per Page
New Search  
Export all 8 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
lumify diagnostic ultrasound system Philips Healthcare K192226 09/06/2019
philips 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 Healthcare K172607 10/04/2017
xperius ultrasound system PHILIPS HEALTHCARE K163020 11/16/2016
lumify ultrasound system Philips Healthcare K162549 10/03/2016
cx50 diagnostic ultrasound system, sparq diagnostic ultrasound system Philips Healthcare K162329 09/14/2016
clearvue850 diagnostic ultrasound system PHILIPS HEALTHCARE K153480 12/16/2015
philips lumify diagnostic ultrasound system PHILIPS HEALTHCARE, INC. K152899 10/30/2015
clearvue 350/550 diagnostic ultrasound system PHILIPS HEALTHCARE K120321 02/17/2012
-
-