FDA 510(k) Applications Submitted by Henry Boland

FDA 510(k) Number Submission Date Device Name Applicant
K110396 02/11/2011 ASPIRA PERITONEAL DRAINAGE SYSTEM C.R. BARD, INC.
K110409 02/14/2011 ASPIRA PLEURAL DRAINAGE SYSTEM C.R. BARD, INC.
K120882 03/23/2012 SITE RITE PREVUE ULTRASOUND SYSTEM AND PINPOINT NEEDLE GUIDE BARD ACCESS SYSTEMS, INC.
K081288 05/07/2008 ASPIRA PERITONEAL DRAINAGE SYSTEM C.R. BARD, INC.
K151698 06/24/2015 BD Angiocath IV Catheter, BD Insyte IV Catheter BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC.
K172204 07/21/2017 BD Intima II PLUS Closed IV Catheter System Becton, Dickinson and Company
K082306 08/13/2008 POWERLOC CLEAR SAFETY INFUSION SET C.R. BARD, INC.
K172506 08/18/2017 BD Cathena Safety IV Catheter Becton, Dickinson and Company
K192493 09/11/2019 BD Cathena (TM) Safety IV Catheter Becton, Dickinson Infusion Therapy Systems, Inc.
K112744 09/21/2011 SAPIENS TIP CONFIRMATION SYSTEM C.R. BARD, INC.
K173354 10/25/2017 BD Nexiva Diffusics Closed IV Catheter Systems Becton Dickinson Infusion Therapy Systems, Inc.
K113808 12/23/2011 THE SHERLOCK 3CG TIP CONFIRMATION SYSTEM (TCS) C.R. BARD, INC.


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