Tri-Med Quick-Step Gastric Lavage Kit

FDA 510(k) K920527 · Tri-Med Specialties, Inc.

Substantially Equivalent

510(k) numberK920527

Submission

Device name
Tri-Med Quick-Step Gastric Lavage Kit
Applicant
Tri-Med Specialties, Inc.
Overland Park, KS, US
Received
February 4, 1992
Decision date
September 4, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KDH – Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

Other 510(k)s with product code KDH

510(k)DeviceApplicantDecision
K983624Giltech Plus Connecting Tube SetKDH · Traditional Giltech Plus, Inc.03/18/1999SE
K981286Superflow Irrigation and Aspiration Tubing SetsKDH · Traditional Armm, Inc.06/19/1998SE
K971259Combiport Fluid Lavage DeviceKDH · Traditional B.Braun Medical, Inc.10/27/1997SE
K962850Tum-E-VacKDH · Traditional Ethox Corp.02/21/1997SE
K951533Easi-Lav Pediatric / Adult Gastric Lavage KitKDH · Traditional Ballard Medical Products07/05/1995SE
K923497Flushing Irrigation SetKDH · Traditional Orion Life Systems, Inc.03/21/1994SESK
K920619Tri-Med Gastric Lavage SystemKDH · Traditional Tri-Med Specialties, Inc.09/04/1992SE
K914908Quicvage PlusKDH · Traditional Autovage04/13/1992SESK
K914907QuicvageKDH · Traditional Autovage01/24/1992SE
K911919Minivage(R)KDH · Traditional Autovage07/26/1991SE

More from Autovage

510(k)DeviceDecision
K971615Pattison Esophageal DilatorKNQ · Traditional 07/24/1997SE
K970890#ES-32 Suction Catheter 32 Fr.KNT · Traditional 05/23/1997SE
K970982T-Rx Retrieval ForcepsOCZ · Traditional 05/09/1997SE
K942918Tri-Med Endoscopic Fluid Introduction CatheterOCX · Traditional 02/28/1995SE
K950574Needle/CannulaLRO · Traditional 02/24/1995SEKD
K934348Tri-Med Quick-Step Gastric Lavage Tube Sizes 18FR, 22FR, 32FRBSS · Traditional 12/23/1994SE
K945160Paracentesis Needles/CannulasLRO · Traditional 11/14/1994SE
K924549Tri-Med Quick-Step(Tm) Rectal TubeGBT · Traditional 02/10/1994SE
K932015Tri-Med Inflatable Esophageal DilatorKNQ · Traditional 02/03/1994SE
K932652Tri-Med Paracentesis TrayLRO · Traditional 11/24/1993SEKD

Questions and answers

When was Tri-Med Quick-Step Gastric Lavage Kit cleared by the FDA?

Tri-Med Quick-Step Gastric Lavage Kit (K920527) received a 510(k) decision of Substantially Equivalent on September 4, 1992, 213 days after the submission was received.

What is the product code of K920527?

The FDA product code is KDH – Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration, a Class II (moderate risk) device regulated under 21 CFR 876.5980.