FDA 510(k) Applications Submitted by C.R. BARD, INC

FDA 510(k) Number Submission Date Device Name Applicant
K151985 07/17/2015 PowerPICC« EtOH Catheter and PowerPICC SOLO«2 EtOH Catheter C.R. Bard, Inc
K162441 08/31/2016 PowerPICC Provena Catheters with SOLO Valve Technology C.R. BARD, INC
K153393 11/24/2015 PowerMidline Catheter C.R. BARD, INC
K161183 04/27/2016 Halo One Thin-Walled Guiding Sheath C.R. BARD, INC
K142443 09/02/2014 Site-Rite 6 Ultrasound System with Pinpoint GT Technology C.R. Bard, Inc
K143208 11/10/2014 Denali Filter System - Femoral Delivery Kit, Denali Filter System - Jugular/Subclavain Delivery Kit C.R. Bard, Inc
K172511 08/21/2017 Hickman TriFusion Catheter C.R. Bard, Inc
K150529 03/02/2015 Site-Rite Prevue Ultrasound System, Site-Rite Prevue+ Ultrasound System C.R. Bard, Inc


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