FDA 510(k) Applications Submitted by MARCIA JOHNSON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120985	04/02/2012	KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING	KIMBERLY-CLARK CORP.
K131254	05/02/2013	KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBE	KIMBERLY-CLARK CORP.
K011713	06/04/2001	SAFESKIN NEON NITRILE - POWDER FREE NEON EXAM GLOVE	KIMBERLY-CLARK CORP.
K141612	06/16/2014	KIMGUARD ONE-STEP STERILIZATION WRAP	KIMBERLY-CLARK HEALTH CARE
K012815	08/22/2001	SAFESKIN HEALTHTOUCH POWDER-FREE EXAM GLOVE WITH VITAMIN E AND ALOE	KIMBERLY-CLARK CORP.
K102666	09/15/2010	KIMBERLY-CLARK SURGICAL DRAPES WITH AAMI LIQUID BARRIER LEVEL 4 CLAIM	KIMBERLY-CLARK CORP.
K093115	10/02/2009	KIMBERLY-CLARK KC100 SURGICAL GOWN, MODEL KC100	KIMBERLY-CLARK CORP.
K113333	11/14/2011	KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS	KIMBERLY-CLARK CORPORATION