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Becton Dickinson Diagnostic Instrument Systems

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K954923BACTEC FUNGAL MEDIUMNovember 21, 1996
K954932BBL MGIT PRODUCTSAugust 21, 1996
K962210BACTEC 9050 SYSTEMAugust 8, 1996
K946268BACTEC(R) 9000TB SYSTEMMay 21, 1996
K960827QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)May 17, 1996
K954921BACTEC STANDARD/10 AEROBIC/F CULTURE VIALSFebruary 16, 1996
K954925BACTEC LYTIC/10 ANAEROBIC/F CULTURE VIALSFebruary 16, 1996
K954927BACTEC PEDS PLUS/F CULTURE VIALSFebruary 16, 1996
K954930BACTEC CULTURE VIALS, LYTIC, ANAEROBICFebruary 16, 1996
K954924BACTEC PEDS PLUS CLUTURE VIALSFebruary 8, 1996
K955504QBC ACCUREAD SYSTEMFebruary 5, 1996
K953340QBC ACCUTUBEOctober 5, 1995
K945205QBC ACCUTUBESeptember 25, 1995