• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • Print
  • Share
  • E-mail
-
31 to 40 of 40 Results
Applicant Cordis US Corporation productcode NIM Decision Date To 10/22/2021
 < 
 1 
 2 
 3 
 4 
 
Records per Page
New Search  
Export all 40 Records to ExcelExport to Excel HelpHelp
Device
Sort by Device [A-Z]
Sort by Device [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
PMA
Number
Sort by PMA Number [0-9]
Sort by PMA Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
cordis precise pro rx nitinol stent system Cordis US Corporation P030047 S013 04/09/2008
cordis precise rx nitinol stent system Cordis US Corporation P030047 S010 01/16/2008
precise nitinol stent system & precise rx nitinol ... Cordis US Corporation P030047 S008 11/30/2007
cordis precise nitinol stent system Cordis US Corporation P030047 S007 11/08/2007
cordis precise nitinol & rx nitinol & pro rx nitin... Cordis US Corporation P030047 S005 09/20/2007
cordis precise otw 5.5 fr and 6.0 fr nitinol stent... Cordis US Corporation P030047 S003 07/12/2007
precise and precise rx nitinol stent systems Cordis US Corporation P030047 S004 06/29/2007
precise and precise rx nitinol stent systems Cordis US Corporation P030047 S002 03/23/2007
cordis precise otw 5.5 fr and 6.0 fr nitinol stent... Cordis US Corporation P030047 S001 11/16/2006
cordis precise nitinol stent system Cordis US Corporation P030047 09/22/2006
-
-