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 2 of 2 Results
ProductCode: FRN Applicant: ABBOTT MFG., INC. Decision Date To: 12/03/2022
Results per Page
New Search  
Export all 2 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]
abbott lifecare standard tubing infusion pump ABBOTT MFG., INC. K965230 07/03/1997
flexiflo quantum enteral pump ABBOTT MFG., INC. K944669 07/24/1995
-
-