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Portex , Ltd.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K040014	PERCUTANEOUS DILATION TRACHEOSTOMY KIT WITH SINGLE STAGE DILATOR AND SOFT INTRODUCERS FOR SIZES 7, 8 AND 9MM TUBES ONLY	JOH	2004-02-13	View
510(k)	K032112	P0RTEX REINFORCED TRACHEAL TUBE (CUFFED AND UNCUFFED)	BTR	2004-01-26	View
510(k)	K033084	WALLACE (SURE VIEW) EMBRYO REPLACEMENT CATHETER AND TRIAL TRANSFER CATHETER	MQF	2003-12-19	View
510(k)	K032716	PORTEX THERMOVENT HEPA HME BREATHING FILTER WITH CO2 PORT (STERILE AND NON-STERILE)	CAH	2003-11-28	View
510(k)	K030570	BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE	BTO	2003-09-17	View
510(k)	K030381	PORTEX BLUE LINE ULTRA TRACHEOSTOMY TUBE (CUFFED) WITH REUSABLE INNER CANNULA	BTO	2003-08-27	View
510(k)	K031622	WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS	MQE	2003-06-26	View

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