• 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
-
121 to 130 of 500 Results *
Decision Date To: 07/22/2019
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 > 
Results per Page
New Search  
Export all 500 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]
vsp orthopedics system 3D Systems, Inc. K190044 08/21/2019
d2p 3D SYSTEMS, INC. K161841 01/09/2017
vsp cranial system 3D Systems, Inc. K151285 09/23/2016
janus i 3D ULTRASOUND, INC. K952551 12/11/1995
janus i 3D ULTRASOUND, INC. K963863 04/21/1997
purzir dental zirconia 3DBioCAD K193055 05/13/2020
3diemme realguide 3DIEMME Ltd. K173041 12/20/2018
computed raddiography scanner 3DISC AMERICAS K102619 05/13/2011
computed radiography scanner 3DISC AMERICAS K133120 01/15/2014
firecr dentalimaging system 3DISC AMERICAS K131442 09/06/2013

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
-
-