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FDA 510(k) Applications Submitted by PASQUALE AMATO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110105
01/13/2011
BD PEN NEEDLE
BECTON DICKINSON AND COMPANY (BD)
K100209
01/25/2010
BD ECLIPSE NEEDLE WITH SMARTSLIP TECHNOLOGY
BECTON DICKINSON & CO.
K021475
05/08/2002
BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET
BD
K131358
05/10/2013
BD PEN NEEDLE
BECTON DICKINSON & CO.
K081446
05/22/2008
BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237
BECTON DICKINSON & CO.
K091758
06/16/2009
BD SPINAL NEEDLE 27G
BECTON DICKSON & CO.
K012584
08/10/2001
MODIFICATION TO: BD DURASAFE PLUS EPIDURAL LOCK CSE NEEDLE SET/KIT
BD
K142821
09/30/2014
PAXgene Blood DNA Tube
PREANALYTIX GMBH
K123300
10/23/2012
BD PEN NEEDLE
BECTON DICKINSON & CO.
K023752
11/08/2002
BD INTEGRA SYRINGE
BD
K153309
11/17/2015
BD Vacutainer UltraTouch Push Button Blood Collection Set
BECTON, DICKINSON AND COMPANY
K043397
12/10/2004
MODIFICATION TO BD ECLIPSE HYPODERMIC NEEDLE
BECTON DICKINSON & CO.
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