FDA 510(k) Applications Submitted by DENNIS MERTZ

FDA 510(k) Number	Submission Date	Device Name	Applicant
K083572	12/03/2008	BD BACTEC PLUS AEROBIC/F BLOOD CULTURE MEDIUM	BECTON, DICKINSON & CO.
K970333	01/28/1997	BACTEC MYCO/F LYTIC CULTURE VIALS	BECTON DICKINSON MICROBIOLOGY SYSTEMS
K970512	02/11/1997	BACTEC MYCO/F LYTIC CULTURE VIALS	BECTON DICKINSON MICROBIOLOGY SYSTEMS
K070691	03/13/2007	BBL CHROMAGAR 0157	BECTON, DICKINSON & CO.
K003062	10/02/2000	BACTEC MGIT 960 SIR KITS	BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
K042812	10/12/2004	BBLCHROMAGAR MRSA	BECTON DICKINSON & CO.
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