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 3 of 3 Results
ProductCode: KDI Applicant: FRESENIUS MEDICAL CARE, NORTH AMERICA Decision Date To: 03/28/2024
Results per Page
New Search  
Export all 3 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]
acetic acid wand, acid wand assembly, bicarbonate wand assembly FRESENIUS MEDICAL CARE, NORTH AMERICA - RENAL THER K133299 07/07/2014
fresenius 2008 hemodiaysis machine with bibag system FRESENIUS MEDICAL CARE, NORTH AMERICA K120017 02/02/2012
fresenius 2008t hemodialysis machine with bibag system FRESENIUS MEDICAL CARE, NORTH AMERICA K121341 12/06/2012
-
-