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 10 of 22 Results
ProductCode: DYB Applicant: CORDIS CORP Decision Date To: 08/25/2016
 
 1 
 2 
 3 
 > 
Results per Page
New Search  
Export all 22 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]
ptca guiding catheter CORDIS CORP. K851947 08/16/1985
cordis catheter sheath introducers,steri-sleeves CORDIS CORP. K855126 02/26/1986
cordis cath sheath introduc/mid-length sheath syst CORDIS CORP. K861082 05/05/1986
entree sheath introducer system CORDIS CORP. K904475 04/01/1991
cordis peel-away insertion tool CORDIS CORP. K910688 05/16/1991
cath sheath introducer syst plus w/unistasis valve CORDIS CORP. K911794 07/19/1991
cordis cath sheath intro syst plus w/unistasis val CORDIS CORP. K913801 10/16/1991
cordis obturator CORDIS CORP. K914352 11/22/1991
cordis nihon catheter sheath introducer CORDIS CORP. K931102 05/27/1993
cordis catheter sheath introducer CORDIS CORP. K932733 08/26/1993
-
-