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