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Becton Dickinson Vacutainer Systems

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002456MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992November 2, 2000
K991702MICROTAINER BRAND CHEMISTRY TUBES WITH MICROGARD CLOSURE, MODEL 365965, 365985, 365963, 365967, 3657July 28, 1999
K991088VACUTAINER BRAND MULTIPLE SAMPLE LUER ADAPTER, BLOOD COLLECTION SETS AND SAFETY-LOK BLOOD COLLECTIONMay 28, 1999
K991120VACUTAINER BRAND CTAD TUBE (MULTIPLE)May 19, 1999
K982541VACUTAINER BRAND ECLIPSE BLOOD COLLECTION NEEDLE, MODELS# 368607 & 368608October 28, 1998
K982922VACUTAINER BRAND BLOOD COLLECTION SYRINGESeptember 22, 1998
K981013VACUTAINER PLUS TUBE WITH EDTA ANTICOAGULANT ANDD VACUTAINER PLUS SERUM TUBEJune 17, 1998
K972075VACUTAINER BRAND PPT PLASMA PREPARATION TUBEFebruary 24, 1998
K980098VACUTAINER BRAND PRONTO NEEDLES HOLDERFebruary 5, 1998
K971449VACUTAINER BRAND PLUS TUBE WITH EDTA ANTICOAGULANT(MULTIPLE)June 17, 1997
K960250VACUTAINER BRAND PLUS SERUM & SST TUBESMarch 29, 1996
K954592VACUTAINER BRAND PST PLASMA SEPARATION TUBENovember 28, 1995
K953994SEDITAINER* ERYTHROCYTE SEDIMENTATION RATE (ESR) SYSTEMSeptember 26, 1995
K953463VACUTAINER PLUS TUBESSeptember 20, 1995
K951886LOK-ON NEEDLE DISPOSAL SYSTEMJune 30, 1995