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Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
632
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K003062BACTEC MGIT 960 SIR KITSJune 6, 2001
K0035530.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGEMarch 21, 2001
K003461BD VACUTAINER PASSIVE SHIELDING BLOOD COLLECTION NEEDLEFebruary 1, 2001
K002938B-D ULTRA-FINE III PEN NEEDLE; MODEL 31G X 3/16November 29, 2000
K001364BD DIRECTIGEN FLU A+BJune 28, 2000
K000762MOXIFLOXACIN, 5 UG, BBL SENSI-DISCApril 25, 2000
K000829GATIFLOXACIN, 5 UG, BBL SENSI-DISCApril 13, 2000
K993186SYNERCID, 15 UG, BBL SENSI-DISCNovember 3, 1999
K992734BECTON DICKINSON SYRINGEOctober 1, 1999
K992849QBC STAR CENTRIFUGAL HEMATOLOGY SYSTEMSeptember 23, 1999
K991551VACUTAINER BRAND SODIUM CITRATE PEDIATRIC TUBESeptember 23, 1999
K984059ANGIOCATH AUTOGUARD CATHETER, INSYTE AUTOGUARD CATHETERApril 9, 1999
K980185COLORPAC TOXIN AJuly 17, 1998
K972728STERILE WATER FOR INJECTION PREFILLED SYRING (SWFIPS)July 15, 1998
K980580BECTON DICKINSON SYRINGESJune 25, 1998
K981797B-D PEN ULTRAJune 12, 1998
K980987BECTON DICKINSON SYRINGEJune 11, 1998
K974363BECTON DICKINSON BLUNT PLASTIC CANNULAJune 3, 1998
K974678B-D AUTO-INJECTORMay 29, 1998
K974883BACTEC MGIT 960 SYSTEMMay 1, 1998