Becton Dickinson Diagnostic Instrument Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Becton Dickinson Diagnostic Instrument Systems - FDA 510(k) Cleared D...
13
Total
13
Cleared
0
Denied
Becton Dickinson Diagnostic Instrument Systems has 13 FDA 510(k) cleared medical devices. Based in Sparks, US.
Historical record: 13 cleared submissions from 1995 to 1996. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Becton Dickinson Diagnostic Instrument Systems Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Becton Dickinson Diagnostic Instrument Systems
13 devices
Cleared
Nov 21, 1996
BACTEC FUNGAL MEDIUM
Microbiology
392d
Cleared
Aug 21, 1996
BBL MGIT PRODUCTS
Microbiology
299d
Cleared
Aug 08, 1996
BACTEC 9050 SYSTEM
Microbiology
59d
Cleared
May 21, 1996
BACTEC(R) 9000TB SYSTEM
Microbiology
515d
Cleared
May 17, 1996
QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)
Hematology
78d
Cleared
Feb 16, 1996
BACTEC STANDARD/10 AEROBIC/F CULTURE VIALS
Microbiology
113d
Cleared
Feb 16, 1996
BACTEC LYTIC/10 ANAEROBIC/F CULTURE VIALS
Microbiology
113d
Cleared
Feb 16, 1996
BACTEC PEDS PLUS/F CULTURE VIALS
Microbiology
113d
Cleared
Feb 16, 1996
BACTEC CULTURE VIALS, LYTIC, ANAEROBIC
Microbiology
113d
Cleared
Feb 08, 1996
BACTEC PEDS PLUS CLUTURE VIALS
Microbiology
105d
Cleared
Feb 05, 1996
QBC ACCUREAD SYSTEM
Hematology
66d
Cleared
Oct 05, 1995
QBC ACCUTUBE
Hematology
80d