Continuous Flow Y-Tubing

FDA 510(k) K010122 · G.U.-Tek

Substantially Equivalent

510(k) numberK010122

Submission

Device name
Continuous Flow Y-Tubing
Applicant
G.U.-Tek
South Plainfield, NJ, US
Received
January 16, 2001
Decision date
June 4, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LJH – System, Irrigation, Urological
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5130
Specialty
Gastroenterology, Urology

Other 510(k)s with product code LJH

510(k)DeviceApplicantDecision
K254111Irrigation/Urology SetsLJH · Traditional B.Braun Medical, Inc.09/10/2026SE
K162992Karl Storz UROMAT E.A.S.I.LJH · Traditional Karl Storz Endoscopy America, Inc.07/07/2017SE
K070873Amsure Bladder Irrigation SetLJH · Traditional Amsino Intl., Inc.12/19/2007SE
K071832Modifcation to: Spyglass Irrigation SystemLJH · Special Medical Scientific, Inc.09/18/2007SE
K063700Spyglass Irrigation SystemLJH · Traditional Medical Scientific, Inc.02/08/2007SE
K062551Nexus Irrigation Tubing SetLJH · Traditional Nexus Medical, LLC12/15/2006SE
K042457Uro ProLJH · Traditional W.O.M. World of Medicine AG10/25/2004SE
K040094Piggyback Irrigating SystemLJH · Abbreviated Kosin Technologies, LLC04/15/2004SE
K023808Irrigation SetsLJH · Traditional International Medsurg Connection03/10/2003SE
K010607Med-Rx Irrigation Set, Model 10-3001, 10-3002, 10-4000, 10-4001LJH · Traditional Benlan, Inc.11/28/2001SE

Questions and answers

When was Continuous Flow Y-Tubing cleared by the FDA?

Continuous Flow Y-Tubing (K010122) received a 510(k) decision of Substantially Equivalent on June 4, 2001, 139 days after the submission was received.

What is the product code of K010122?

The FDA product code is LJH – System, Irrigation, Urological, a Class II (moderate risk) device regulated under 21 CFR 876.5130.