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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 10 of 13 Results
ProductCode: FMI Applicant: VIDACARE CORPORATION Decision Date To: 12/08/2022
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ez-io intraosseous infusion system VIDACARE CORPORATION K132583 02/11/2014
the t.a.l.o.n. intraossous infusion system by vidacre VIDACARE CORPORATION K120661 06/03/2012
powered pd-io infusion system, ez-io humeral head, powered ph-io VIDACARE CORPORATION K101026 07/27/2010
ez-mio distal tibia, ez-io distal tibia, vidaport intraosseous infusion system, ez-io VIDACARE CORPORATION K091140 10/14/2009
ez-mio sternal VIDACARE CORPORATION K063567 01/26/2007
manual pd-io; powered pd-io VIDACARE CORPORATION K063142 12/08/2006
ez-mio, ez-io distal tibia VIDACARE CORPORATION K062956 12/05/2006
humeral head, manual driver VIDACARE CORPORATION K062422 11/07/2006
ez-io VIDACARE CORPORATION K052408 11/17/2005
ez-mio manual driver VIDACARE CORPORATION K052195 11/02/2005