Portex , Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Portex , Ltd. has 7 FDA 510(k) cleared medical devices. Based in England Ct21 6db, GB.
Historical record: 7 cleared submissions from 2003 to 2004. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Portex , Ltd. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Feb 13, 2004
PERCUTANEOUS DILATION TRACHEOSTOMY KIT WITH SINGLE STAGE DILATOR AND SOFT...
Anesthesiology
51d
Cleared
Jan 26, 2004
P0RTEX REINFORCED TRACHEAL TUBE (CUFFED AND UNCUFFED)
Anesthesiology
201d
Cleared
Dec 19, 2003
WALLACE (SURE VIEW) EMBRYO REPLACEMENT CATHETER AND TRIAL TRANSFER CATHETER
Obstetrics & Gynecology
81d
Cleared
Nov 28, 2003
PORTEX THERMOVENT HEPA HME BREATHING FILTER WITH CO2 PORT (STERILE AND...
General Hospital
87d
Cleared
Sep 17, 2003
BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE
Anesthesiology
205d
Cleared
Aug 27, 2003
PORTEX BLUE LINE ULTRA TRACHEOSTOMY TUBE (CUFFED) WITH REUSABLE INNER CANNULA
Anesthesiology
203d
Cleared
Jun 26, 2003
WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS
Obstetrics & Gynecology
34d