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.