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Portex , Ltd.

7 FDA 510(k) clearances · Manufacturer

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

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Every clearance here is in the API, with alerts when new ones post.