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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 22 Results
ProductCode: LJT Applicant: C.R. BARD, INC. Decision Date To: 04/26/2024
 
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Export all 22 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
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x-prot duo port C.R. BARD, INC. K032044 07/10/2003
titanium powerport isp implanted port with 6 fr chronoflex polyurethane catheter C.R. BARD, INC. K072549 11/14/2007
titanium powerport isp implanted port C.R. BARD, INC. K072215 11/01/2007
powerport(tm)implanted titanium port w/8 fr. chronoflex catheter-multiple C.R. BARD, INC. K060812 07/14/2006
powerport polymetric port with 8 fr s/l chronoflex catheter C.R. BARD, INC. K063377 01/25/2007
powerport implanted port with groshong catheter C.R. BARD, INC. K081311 06/04/2008
powerport implantable port C.R. BARD, INC. K133335 02/14/2014
powerport duo m.r.i. implanted port with 9.5 fr. dual lumen chronoflex polyurethane catheter C.R. BARD, INC. K090512 03/27/2009
powerport clearvue slim implantable port C.R. BARD, INC. K122899 11/15/2012
power-injectable implantable ports with chronoflex polyurethane catheters C.R. Bard, Inc. K150514 11/20/2015
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