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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