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FDA 510(k) Applications Submitted by John 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.
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