Karl Storz UROMAT E.A.S.I.

FDA 510(k) K162992 · Karl Storz Endoscopy America, Inc.

Substantially Equivalent

510(k) numberK162992

Submission

Device name
Karl Storz UROMAT E.A.S.I.
Applicant
Karl Storz Endoscopy America, Inc.
El Segundo, CA, US
Received
October 27, 2016
Decision date
July 7, 2017
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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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 Karl Storz UROMAT E.A.S.I. cleared by the FDA?

Karl Storz UROMAT E.A.S.I. (K162992) received a 510(k) decision of Substantially Equivalent on July 7, 2017, 253 days after the submission was received.

What is the product code of K162992?

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