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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
K954927BACTEC PEDS PLUS/F CULTURE VIALSFebruary 16, 1996
K954930BACTEC CULTURE VIALS, LYTIC, ANAEROBICFebruary 16, 1996
K954925BACTEC LYTIC/10 ANAEROBIC/F CULTURE VIALSFebruary 16, 1996
K954924BACTEC PEDS PLUS CLUTURE VIALSFebruary 8, 1996
K955504QBC ACCUREAD SYSTEMFebruary 5, 1996
K953340QBC ACCUTUBEOctober 5, 1995
K945205QBC ACCUTUBESeptember 25, 1995