Portex , Ltd.
Portex , Ltd. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2004.
Top product codes for Portex , Ltd.
Recent clearances by Portex , Ltd.
- K040014 — PERCUTANEOUS DILATION TRACHEOSTOMY KIT WITH SINGLE STAGE DILATOR AND SOFT INTRODUCERS FOR SIZES 7, 8 AND 9MM TUBES ONLY
- K032112 — P0RTEX REINFORCED TRACHEAL TUBE (CUFFED AND UNCUFFED)
- K033084 — WALLACE (SURE VIEW) EMBRYO REPLACEMENT CATHETER AND TRIAL TRANSFER CATHETER
- K032716 — PORTEX THERMOVENT HEPA HME BREATHING FILTER WITH CO2 PORT (STERILE AND NON-STERILE)
- K030570 — BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE
- K030381 — PORTEX BLUE LINE ULTRA TRACHEOSTOMY TUBE (CUFFED) WITH REUSABLE INNER CANNULA
- K031622 — WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS
Data sourced from openFDA. This site is unofficial and independent of the FDA.