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
-
11 to 20 of 30 Results
ProductCode: FPA Applicant: ABBOTT LABORATORIES Decision Date To: 02/22/2017
 < 
 1 
 2 
 3 
 > 
Results per Page
New Search  
Export all 30 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]
lifeshield anesthesia set ABBOTT LABORATORIES K913982 11/05/1992
monoplace hyperbaric extension set (l 11055) ABBOTT LABORATORIES K884141 02/28/1989
venovalve(tm) ABBOTT LABORATORIES K881234 06/13/1988
quik lok ABBOTT LABORATORIES K840878 03/30/1984
venoset multi-med piggyback w/ivex-2 ABBOTT LABORATORIES K833740 12/27/1983
venoset multi med dual rate piggyback ABBOTT LABORATORIES K833741 12/22/1983
venipuncture valve ABBOTT LABORATORIES K832123 08/12/1983
venoset dual-rate piggyback w/ivex & ABBOTT LABORATORIES K821578 06/22/1982
vented nitroglycerin i.v. set ABBOTT LABORATORIES K821515 06/09/1982
vented primary piggyback venoset dual ABBOTT LABORATORIES K810239 05/29/1981
-
-