• 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 12 Results
ProductCode: FPA Applicant: HOSPIRA, INC Decision Date To: 03/03/2015
Results per Page
New Search
Export all 12 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]
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
plum 360 infusion system with hospira me hospira, inc. K141789 01/16/2015
iv administration hospira, inc. K142622 01/15/2015
extension sets hospira, inc K142974 01/09/2015
hospira extension set hospira, inc. K142433 12/08/2014
hospira primary sets hospira, inc. K142367 11/25/2014
primary symbiq set, dital microbore tubi hospira, inc. K121032 06/21/2012
symbiq infusion and adminstration set hospira, inc. K110901 03/05/2012
hospira plum infusion set; hospira infus hospira, inc. K103224 01/07/2011
infusion sets hospira, inc. K103344 12/10/2010
hospira infusion blood sets hospira, inc. K101677 08/11/2010