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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 18 of 18 Results
ProductCode: FPA Applicant: HOSPIRA, INC Decision Date To: 05/27/2016
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hospira primary sets HOSPIRA, INC. K142367 11/25/2014
primary symbiq set, dital microbore tubing, 0.2 micron filter, non-dehp HOSPIRA, INC. K121032 06/21/2012
symbiq infusion and adminstration set HOSPIRA, INC. K110901 03/05/2012
hospira plum infusion set; hospira infusion set with yellow stripe tubing HOSPIRA, INC. K103224 01/07/2011
infusion sets HOSPIRA, INC. K103344 12/10/2010
hospira infusion blood sets HOSPIRA, INC. K101677 08/11/2010
lifeshield latex-free gravitech flow controller i.v. sets, models 17528, 17527, 17525 & 17526 HOSPIRA, INC. K063239 12/11/2006
lifeshield latex-free microbore extension set, model 14949 and others HOSPIRA, INC. K052722 11/02/2005
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