FDA 510(k) Applications Submitted by KATHERINE M WORTLEY

FDA 510(k) Number	Submission Date	Device Name	Applicant
K142792	09/26/2014	AbbVie NJ	ABBVIE INC.
K142793	09/26/2014	AbbVie PEG	AbbVie Inc.
K142816	09/29/2014	AbbVie J	ABBVIE INC.
K133087	09/30/2013	ABBVIE PEG	ABBVIE INC.
K133096	09/30/2013	ABB VIE J	ABBVIE INC.
K133129	09/30/2013	ABBVIE NJ	ABBVIE INC.
K990373	02/08/1999	FACT PLUS ONE STEP PREGNANCY TEST	ABBOTT LABORATORIES
K991483	04/28/1999	ABBOTT ARCHITECT GLYCATED HEMOGLOBIN	ABBOTT LABORATORIES
K992085	06/21/1999	ABBOTT IMX GLYCATED HEMOGLOBIN II	ABBOTT LABORATORIES
K992710	08/11/1999	ABBOTT ARCHITECH GLYCATED HEMOGLOBIN MASTERCHECK	ABBOTT LABORATORIES