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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 7 of 7 Results
ProductCode: FPA Applicant: HOSPIRA, INC Decision Date To: 09/18/2014
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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
lifeshield latex-free gravitech flow con hospira, inc. K063239 12/11/2006
lifeshield latex-free microbore extensio hospira, inc. K052722 11/02/2005
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