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FDA 510(k) Applications Submitted by BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K954923
10/26/1995
BACTEC FUNGAL MEDIUM
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K954924
10/26/1995
BACTEC PEDS PLUS CLUTURE VIALS
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K954925
10/26/1995
BACTEC LYTIC/10 ABAERIBIC/F CULTURE VIALS
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K954921
10/26/1995
BACTEC STANDARD/10 AEROBIC/F CULTURE VIALS
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K954927
10/26/1995
BACTEC PEDS PLUS/F CULTURE VIALS
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K954930
10/26/1995
BACTEC CULTURE VIALS, LYTIC, ANAEROBIC
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K954932
10/27/1995
BBL MGIT PRODUCTS
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K946268
12/23/1994
BACTEC(R) 9000TB SYSTEM
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K962210
06/10/1996
BACTEC 9050 SYSTEM
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K960827
02/29/1996
QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
K955504
12/01/1995
QBC ACCUREAD SYSTEM
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
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