Tri-Med Quick-Step Gastric Lavage Kit

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K920527 ↗

FDA Product Code

KDH

Device Class

Class II

Regulation

21 CFR Part 876.5980

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Tri-Med Paracentesis Tray

  Class II

  FDA 510(k) K932652 Active Cleared 24 Nov 1993

• T-Rx Retrieval Forceps

  Class II

  FDA 510(k) K970982 Active Cleared 9 May 1997

• Paracentesis Needles/Cannulas

  Class II

  FDA 510(k) K945160 Active Cleared 14 Nov 1994

• Pattison Esophageal Dilator

  Class II

  FDA 510(k) K971615 Active Cleared 24 Jul 1997

• Tri-Med Gastric Lavage System

  Class II

  FDA 510(k) K920619 Active Cleared 4 Sep 1992

• Tri-Med Endoscopic Fluid Introduction Catheter

  Class II

  FDA 510(k) K942918 Active Cleared 28 Feb 1995

See all devices from Tri-Med Specialties, Inc. →