FDA 510(k) Applications Submitted by RICHARD WANG

FDA 510(k) Number	Submission Date	Device Name	Applicant
K971122	03/27/1997	ACCULINE PREGNANCY TEST	GENIX BIOTEK, INC.
K964633	11/19/1996	ACCUPACK PREGNANCY TEST	GENIX BIOTEK, INC.
K991215	04/09/1999	SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S	SYMTEX HEALTHCARE CORP.