FDA 510(k) Applications Submitted by GEORGE M TANCOS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020208	01/22/2002	GLUCOMETER ELITE DIABETES CARE SYSTEM (MODIFIED)	BAYER GROUP DIAGNOSTICS
K020210	01/22/2002	GLUCOMETER DEX BLOOD GLUCOSE SYSTEM (MODIFIED)	BAYER GROUP DIAGNOSTICS
K990649	03/01/1999	GLUCOMETER ELITE XL BLOOD GLUCOSE METER, GLUCOMETER ELITE BLOOD GLUCOSE TEST SYSTEMS	BAYER CORP.
K991242	04/12/1999	GLUCOMETER ELITE TEST STRIPS	BAYER CORP.
K991315	04/19/1999	MICROALBUSTIX REAGENT STRIPS (OTC)	BAYER CORP.
K012205	07/16/2001	GLUCOMETER DEX TEST SENSOR	BAYER CORP.
K984006	11/10/1998	GLUCOMETER ELITE XL BLOOD GLUCOSE METER	BAYER CORP.
K043158	11/15/2004	ASCENSIA BRIO BLOOD GLUCOSE MONITORING SYSTEM	BAYER HEALTHCARE, LLC
K043311	12/01/2004	ASCENSIA ELITE DIABETES CARE SYSTEM	BAYER HEALTHCARE, LLC
K024062	12/09/2002	ASCENSIA BREEZE BLOOD GLUCOSE METER	BAYER CORP.
K024234	12/23/2002	ASCENSIA GLUCOFACTS; ASCENSIA GLUCOFACTS PROFESSIONAL	BAYER CORP.