FDA 510(k) Applications Submitted by GREG W MORGAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K982558	07/22/1998	BD PREEFILE NORMAL SALINE FLUSH SYRINGE FLUSH SYRINGE	BD/PREEFIL
K992734	08/13/1999	BECTON DICKINSON SYRINGE	BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
K010188	01/22/2001	BD ECLIPSE HYPODERMIC NEEDLE	BD MEDICAL SYSTEMS
K011103	04/11/2001	BD SPRING BASED SYRINGE	BD
K980987	03/17/1998	BECTON DICKINSON SYRINGE	BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
K011858	06/14/2001	INTERLINK THREADED LOCK CANNULA	BD
K011967	06/25/2001	BD PRE-FILLED HEPARIN LOCK FLUSH IN 0.9% SODIUM CHLORIDE INJECTION, USP SYRINGE	BD
K011982	06/26/2001	0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE	BD
K954953	10/30/1995	B-D DURASAFE COMBINED SPINAL EPIDURAL (CSE) TRAY	BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
K003553	11/17/2000	0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE	BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
K974363	11/19/1997	BECTON DICKINSON BLUNT PLASTIC CANNULA	BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
K964654	11/20/1996	BECTON DICKINSON BLUNT PLASTIC CANNULA	BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC