• 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 13 Results
ProductCode: DWF Applicant: Medtronic, Inc. Decision Date To: 05/01/2024
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 13 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]
dlp silicone coronary artery ostial cannulae Medtronic, Inc. K231206 12/07/2023
dlp™ silicone coronary artery ostial cannulae Medtronic, Inc. K230960 05/04/2023
bio-medicus insertion kit Medtronic, Inc. K190557 04/03/2019
dlp aortic root cannula, dlp aortic root cannula with vent line, dlp pressure monitoring extension line adapter, dlp cardioplegia adapter with pressure port Medtronic, Inc. K182586 10/19/2018
tubing pack Medtronic, Inc. K171979 10/27/2017
tubing pack Medtronic, Inc. K171308 06/02/2017
uncoated tubing and connector components MEDTRONIC, INC. K151523 07/16/2015
medtronic bio-medicus cannula insertion kit Medtronic, Inc. K150567 04/09/2015
eopa 3d arterial cannula MEDTRONIC, INC. K150422 03/20/2015
dlp vein graft cannula MEDTRONIC, INC. K143107 01/07/2015
-
-