FDA 510(k) Applications Submitted by K C YEE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K061257	05/04/2006	DBEST HCG PANEL TEST KIT	AMERITEK USA, INC.
K983188	09/11/1998	DBEST TETRAHYDROCANNABINOL TEST KIT	AMERITEK, INC.
K983189	09/11/1998	DBEST METHAMPHETAMINES TEST KIT	AMERITEK, INC.
K983190	09/11/1998	DBEST OPIATES TEST KIT	AMERITEK, INC.
K983191	09/11/1998	DBEST COCAINE TEST KIT	AMERITEK, INC.
K973957	10/16/1997	DBEST ONE-STEP HCG SERUM/URINE TEST	AMERITEK, INC.
K984269	10/22/1998	DBEST OCCULT BLOOD TEST KIT	AMERITEK, INC.
K990681	03/02/1999	DBSET MULTIDRUG SCREEN TEST KIT	AMERITEK, INC.
K990873	03/16/1999	DBEST URINARY TRACT INFECTION TEST KIT FOR HOME-USE	AMERITEK, INC.
K001215	04/14/2000	DBEST HCG 2 IU/ML TEST KIT	AMERITEK, INC.
K981504	04/27/1998	DBEST AMPHETAMINES TEST KIT	AMERITEK, INC.
K071242	05/03/2007	DBEST ONE STEP OCCULT BLOOD TEST KITS	AMERITEK USA, INC.
K973142	08/21/1997	DBEST REAGENT STRIP FOR URINALYSIS	AMERITEK, INC.
K050352	02/11/2005	IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT	AMERITEK RESEARCH LLC
K974508	12/01/1997	DBEST ONE-STEP OVULATION TEST	AMERITEK, INC.