Uro Pro

FDA 510(k) K042457 · W.O.M. World of Medicine AG

Substantially Equivalent

510(k) numberK042457

Submission

Device name
Uro Pro
Applicant
W.O.M. World of Medicine AG
Hingham, MA, US
Received
September 10, 2004
Decision date
October 25, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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

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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
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
K010122Continuous Flow Y-TubingLJH · Traditional G.U.-Tek06/04/2001SE

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Questions and answers

When was Uro Pro cleared by the FDA?

Uro Pro (K042457) received a 510(k) decision of Substantially Equivalent on October 25, 2004, 45 days after the submission was received.

What is the product code of K042457?

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