FDA 510(k) Applications Submitted by STEVE OGILVIE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K030381	02/05/2003	PORTEX BLUE LINE ULTRA TRACHEOSTOMY TUBE (CUFFED) WITH REUSABLE INNER CANNULA	PORTEX LTD.
K030570	02/24/2003	BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE	PORTEX LTD.
K031622	05/23/2003	WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS	PORTEX LTD.
K022212	07/08/2002	PORTEX PERCUTANEOUS DILATATIONAL TRACHEOSTOMY KITS	MENTOR MEDICAL LIMITED
K032112	07/09/2003	P0RTEX REINFORCED TRACHEAL TUBE (CUFFED AND UNCUFFED)	PORTEX LTD.
K032716	09/02/2003	PORTEX THERMOVENT HEPA HME BREATHING FILTER WITH CO2 PORT (STERILE AND NON-STERILE)	PORTEX LTD.
K033084	09/29/2003	WALLACE (SURE VIEW) EMBRYO REPLACEMENT CATHETER AND TRIAL TRANSFER CATHETER	PORTEX LTD.
K012277	07/19/2001	PORTEX RING PESSARY PVC-NON STERILE; PORTEX RING PESSARY POLYTHENE- NON STERILE	SIMS PORTEX LTD.
K001555	05/18/2000	SURESAMPLE-WALLACE ENDOMETRIAL SAMPLER, ENDO 26	SIMS PORTEX LTD.