Cysto-Urethroscopes E-Line Existing of: Sheaths, Obturators, Inserts, Attchements, and Forceps Model 8650, 8652, 8660

FDA 510(k) K011496 · Richard Wolf Medical Instruments Corp.

Substantially Equivalent

510(k) numberK011496

Submission

Device name
Cysto-Urethroscopes E-Line Existing of: Sheaths, Obturators, Inserts, Attchements, and Forceps Model 8650, 8652, 8660
Applicant
Richard Wolf Medical Instruments Corp.
Vernon Hills, IL, US
Received
May 15, 2001
Decision date
August 10, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FBO – Cystourethroscope
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

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K243409KARL STORZ Pediatric Cysto-Urethro-Fiberscope (11274BCU1)FBO · Special Karl Storz SE & CO. KG11/27/2024SE
K131364Flexible Cmos-Video-Cysto-UrethroscopeFBO · Traditional KARL STORZ Endoscopy-America, Inc.01/02/2014SE
K082046Karl Storz Pediatric Flexible Cysto-Urethro-Fiberscope, Model 11278C1/ACUI and Circon…FBO · Traditional KARL STORZ Endoscopy-America, Inc.10/10/2008SE
K080780Anchorage Scope, Model 000003FBO · Traditional Epitek, Inc.07/30/2008SE
K062918Karl Storz Flexible Video-Urethro-Cystoscope SystemFBO · Traditional KARL STORZ Endoscopy-America, Inc.01/17/2007SE
K061646Laserscope Guided Delivery Device (GDD) Cystourethroscope & AccessoriesFBO · Traditional Laserscope06/27/2006SE
K972979Smith & Nephew Images Cystourethroscopes and Accessories, Smith & Nephew SEMI0RIGID and…FBO · Traditional Smith & Nephew, Inc.12/11/1997SE
K962474Olympus FG Series of Rat Tooth Grasping Forceps (Urology)FBO · Traditional Olympus America, Inc.12/20/1996SE
K941992CystoscopeFBO · Traditional Surgical Technologies, Inc.11/30/1995SE

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Questions and answers

When was Cysto-Urethroscopes E-Line Existing of: Sheaths, Obturators, Inserts, Attchements, and Forceps Model 8650, 8652, 8660 cleared by the FDA?

Cysto-Urethroscopes E-Line Existing of: Sheaths, Obturators, Inserts, Attchements, and Forceps Model 8650, 8652, 8660 (K011496) received a 510(k) decision of Substantially Equivalent on August 10, 2001, 87 days after the submission was received.

What is the product code of K011496?

The FDA product code is FBO – Cystourethroscope, a Class II (moderate risk) device regulated under 21 CFR 876.1500.