Medical Device Manufacturer · GB , England Ct21 6db

Portex , Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2003

Recent clearances: PERCUTANEOUS DILATION TRACHEOSTOMY KIT WITH SINGLE STAGE DILATOR AND SOFT INTRODUCERS FOR SIZES 7, 8 AND 9MM TUBES ONLY, P0RTEX REINFORCED TRACHEAL TUBE (CUFFED AND UNCUFFED), WALLACE (SURE VIEW) EMBRYO REPLACEMENT CATHETER AND TRIAL TRANSFER CATHETER

View 7 510(k) Devices ↓

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Portex , Ltd. General Hospital ✕

1 devices

1-1 of 1

Cleared Nov 28, 2003

PORTEX THERMOVENT HEPA HME BREATHING FILTER WITH CO2 PORT (STERILE AND...

General Hospital · 87d