Medical Device Manufacturer · GB , England Ct21 6db

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

7 submissions · 7 cleared · Since 2003

7

Total

7

Cleared

0

Denied

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

4 devices

1-4 of 4

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 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