Karl Storz Uretero-Renoscope/Ureterscope

FDA 510(k) K940464 · KARL STORZ Endoscopy-America, Inc.

Substantially Equivalent

510(k) numberK940464

Submission

Device name
Karl Storz Uretero-Renoscope/Ureterscope
Applicant
KARL STORZ Endoscopy-America, Inc.
Washington, D.C., DC, US
Received
February 2, 1994
Decision date
June 24, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FGB – Ureteroscope And Accessories, Flexible/Rigid
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To perform various diagnostic and therapeutic procedures within the urinary tract. For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Other 510(k)s with product code FGB

510(k)DeviceApplicantDecision
K262488Single-Use Video Flexible Ureterorenoscope (RP-U-C06R9, RP-U-C06R3, RP-U-C06S9…FGB · Traditional Guangzhou Red Pine Medical Instrument Co., Ltd.09/09/2026SE
K261153LithoVue Elite Digital Flexible Ureteroscope SystemFGB · Traditional Boston Scientific Corporation08/26/2026SE
K262552Single-use Flexible Ureteroscope (Single-use Flexible Ureteroscope: SUV-5C-B)FGB · Special Scivita Medical Technology Co., Ltd.08/14/2026SE
K253505Zamenix™ PFGB · Traditional Roen Surgical, Inc.08/07/2026SE
K260516BubbleView Single-Use Digital Flexible Cystoscope (C38-CS, C38-CRS, C50-C, C50-CR…FGB · Traditional MacroLux Medical Technology Co., Ltd.07/20/2026SE
K252929Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model…FGB · Traditional Anhui Happiness Workshop Instruments Co., Ltd.04/09/2026SE
K260013CVAC Image ProcessorFGB · Traditional Calyxo, Inc.03/06/2026SE
K252468Single-use Digital Flexible Ureteroscope (GY-UR9.3); Single-use Digital Flexible…FGB · Traditional Zhejiang Geyi Medical Instrument Co., Ltd.12/16/2025SE
K251951Single-Use Video Flexible Ureterorenoscope (RP-U-C03R9, RP-U-C03R3, RP-U-C03S9…FGB · Traditional Guangzhou Red Pine Medical Instrument Co., Ltd.12/16/2025SE
K253411Miniature Telescope for Urology (27033AA)FGB · Traditional Karl Storz SE & CO. KG11/18/2025SE

More from Karl Storz SE & CO. KG

510(k)DeviceDecision
K252624KARL STORZ Laryngoscopes and AccessoriesEQN · Traditional 05/15/2026SE
K240506KARL STORZ HoldersOCV · Traditional 10/22/2024SE
K223885HOPKINS TelescopesHIH · Traditional 09/14/2023SE
K230359KOH Ultramicro Injection Cannula (26167NN); Suction a. Irrig. Cannula,L. 36cm (37360CP)…GCJ · Traditional 06/23/2023SE
K223520UNIDRIVE SIII SystemHIH · Traditional 04/27/2023SE
K223923HOPKINS TelescopesGCJ · Traditional 03/30/2023SE
K221893KARL STORZ Bipolar Resectoscopes with HF CableFJL · Traditional 03/17/2023SE
K221004HOPKINS TelescopesGCJ · Traditional 12/20/2022SE
K222504H1GCJ · Traditional 11/10/2022SE
K213194HD MediastinoscopeEWY · Traditional 06/23/2022SE

Questions and answers

When was Karl Storz Uretero-Renoscope/Ureterscope cleared by the FDA?

Karl Storz Uretero-Renoscope/Ureterscope (K940464) received a 510(k) decision of Substantially Equivalent on June 24, 1994, 142 days after the submission was received.

What is the product code of K940464?

The FDA product code is FGB – Ureteroscope And Accessories, Flexible/Rigid, a Class II (moderate risk) device regulated under 21 CFR 876.1500.