A-Port Implantable Vascular Access System Line Ext

• • Terminated Z-0285-2007 FDA Unclassified (pre-2012) ·initiated 29 Sep 2006

  Catheter has separated from the infusion port body.

510(k) Number

K921379 ↗

FDA Product Code

LJT

Device Class

Class II

Regulation

21 CFR Part 880.5965

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Non-Corning (Huber) Needle

  Class II

  FDA 510(k) K936029 Active Cleared 4 Feb 1994

• A-Port Implant Vasc Access Syst Line Ext-A2 Port

  Class II

  FDA 510(k) K911055 Active Cleared 19 Apr 1991

• Therex Low-Profile Port 1.5mm I.D. X 2.7mm O.D. Detached Catheter System

  Class II

  FDA 510(k) K933350 Active Cleared 23 Feb 1994

• Low Profile Titanium Model Catalog #1003

  Class II

  FDA 510(k) K953110 Active Cleared 13 Sep 1995

• A Port Implant Vascular Access System - Detached

  Class II

  FDA 510(k) K882230 Active Cleared 29 Jul 1988

• Therex Low-Profile Port - Titanium Model

  Class II

  FDA 510(k) K942412 Active Cleared 19 Aug 1994

See all devices from Therex Corp. →