• 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
-
11 to 14 of 14 Results
ProductCode: KDI Applicant: GAMBRO, INC. Decision Date To: 05/01/2024
 < 
 1 
 2 
 
Results per Page
New Search  
Export all 14 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]
fh 101, fh 202 & fh 303 fiber hemofilter GAMBRO, INC. K830284 03/02/1983
gambro lundia plate high flux dialyzer GAMBRO, INC. K811944 08/31/1981
gambro lundia major high flux hemodialyz GAMBRO, INC. K801480 08/27/1980
gambro lundia plate high flux hemodial- GAMBRO, INC. K801479 08/27/1980
-
-