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 10 of 18 Results
ProductCode: FPA Applicant: HOSPIRA, INC Decision Date To: 12/08/2016
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 18 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 latex-free microbore extension set, model 14949 and others HOSPIRA, INC. K052722 11/02/2005
lifeshield latex-free gravitech flow controller i.v. sets, models 17528, 17527, 17525 & 17526 HOSPIRA, INC. K063239 12/11/2006
hospira infusion blood sets HOSPIRA, INC. K101677 08/11/2010
infusion sets HOSPIRA, INC. K103344 12/10/2010
hospira plum infusion set; hospira infusion set with yellow stripe tubing HOSPIRA, INC. K103224 01/07/2011
symbiq infusion and adminstration set HOSPIRA, INC. K110901 03/05/2012
primary symbiq set, dital microbore tubing, 0.2 micron filter, non-dehp HOSPIRA, INC. K121032 06/21/2012
hospira primary sets HOSPIRA, INC. K142367 11/25/2014
hospira extension set Hospira, Inc. K142433 12/08/2014
extension sets Hospira, Inc K142974 01/09/2015
-
-