Dual Plastic Vascular Access System

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K922147 ↗

FDA Product Code

LJT

Device Class

Class II

Regulation

21 CFR Part 880.5965

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Gerard Medical, Inc. Trim-Port

  Class II

  FDA 510(k) K903364 Active Cleared 31 Oct 1990

• Modified Version Implantable Vascular Access Syste

  Class II

  FDA 510(k) K912111 Active Cleared 8 Oct 1991

• Trimport

  Class II

  FDA 510(k) K942623 Active Cleared 23 Aug 1994

• Trim-Port(Tm) Implant Access Syst Dual Titan Port

  Class II

  FDA 510(k) K913114 Active Cleared 2 Jan 1992

• Gerard Medical Electrode Tester

  Class II

  FDA 510(k) K813358 Active Cleared 29 Dec 1981

• Trimport Implantable Access System (Modification)

  Class II

  FDA 510(k) K954258 Active Cleared 24 May 1996

See all devices from Gerard Medical Enterprises, Inc. →