Cath-Tech Port Implantable Vascular Access System

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

510(k) Number

K880571 ↗

FDA Product Code

LJT

Device Class

Class II

Regulation

21 CFR Part 880.5965

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Groshong Cv Catheter Repair Kit Open recall

  Class II

  FDA 510(k) K871998 Active Cleared 24 Jun 1987

• Testcorp Preg

  Class II

  FDA 510(k) K831366 Active Cleared 2 Jun 1983

• Brawn and Groshong Catheters

  Class II

  FDA 510(k) K860256 Active Cleared 28 Mar 1986

• Cath-Tech Polyurethane Umbilical Vess

  Class II

  FDA 510(k) K842577 Active Cleared 13 Mar 1985

• Umbilical Vessel Catheter

  Class II

  FDA 510(k) K840339 Active Cleared 25 Jul 1984

• Peripherally Inserted Central Venous Catheter

  Class II

  FDA 510(k) K871080 Active Cleared 12 Aug 1987

See all devices from Catheter Technology Corp. →