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FDA 510(k) Applications Submitted by GREGORY MORGAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
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
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