FDA 510(k) Applications Submitted by JOHN A ROBERTS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130197	01/28/2013	BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55	Becton, Dickinson and Company
K120384	02/07/2012	PROTECTOR, INJECTOR, CONNECTOR	BD MEDICAL-MEDICAL SURGICAL SYSTEMS
K140591	03/07/2014	BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - INJECTOR	BECTON DICKINSON & CO.
K090680	03/16/2009	HEPARIN LOCK FLUSH SOLUTION, USP BD POSIFLUSH HEPARIN LOCK FLUSH SYRINGE	BECTON DICKINSON & CO.
K110771	03/21/2011	BD SINGLE USE, HYPODERMIC SYRINGE	Becton, Dickinson and Company
K121050	04/06/2012	0.9% SODIUM CHLORIDE INJECTION USP BD POSIFLUSH FLUSH SYRINGE, SF FLUSH SYRINGE	BECTON DICKINSON & CO.
K112434	08/24/2011	BD ORAL/ENTERAL SYRINGE WITH BD UNIVIA CONNECTION	BD MEDICAL SURGICAL
K123213	10/15/2012	BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE	BECTON DICKINSON & CO.
K143610	12/19/2014	BD INTIMA II CLOSED IV CATHETER	Becton Dickinson Infusion Therapy Systems Inc.
K960647	02/15/1996	OMEGA TOTAL HIP SYSTEM FOR CEMENTED APPLICATIONS	OSTEOIMPLANT TECHNOLOGY, INC.