• 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
-
41 to 50 of 500 Results *
Decision Date To: 07/22/2019
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
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]
simmetry sacroiliac joint fusion system Zyga Technology, Inc. K151818 08/05/2015
simmetry(tm) sacroiliac joint fusion system Zyga Technology, Inc. K111801 07/21/2011
simmetry sacroiliac joint fusion system Zyga Technology, Inc. K141549 01/15/2015
coagcare anticoagulation management system ZYCARE K050821 08/16/2005
diazir ZXTGY (BEIJING) TECHNOLOGY CO., LTD K161652 11/28/2017
zutron medical endoscope leak tester model zutr-10003 ZUTRON MEDICAL LLC K093718 02/22/2010
zutron colonoscope stiffening device ZUTRON MEDICAL K051068 07/11/2005
zurich pressure guidewire system model 100 Zurich Medical Inc. K190852 08/14/2019
z-ray intra-oral digital radiography system ZUMA DENTAL, LLC K133206 05/13/2014
ceramibond ZULAUF, INC. K802899 12/19/1980

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