Video Ureteroscope System

FDA 510(k) K231135 · Hunan Vathin Medical Instrument Co., Ltd.

Substantially Equivalent

510(k) numberK231135

Submission

Device name
Video Ureteroscope System
Applicant
Hunan Vathin Medical Instrument Co., Ltd.
Xiangtan, CN
Received
April 21, 2023
Decision date
January 17, 2024
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
K250232Vathin® Video Bronchoscope SystemEOQ · Traditional 07/25/2025SE
K251599Single-use Ureteral Access SheathFED · Special 07/03/2025SE
K250785Single-use Flexible UreteroscopeFGB · Traditional 05/06/2025SE
K243117Digital Video ProcessorFGB · Traditional 01/29/2025SE
K242416Single-use Flexible Bronchoscope: BC-E1C10, BC-E1C11, BC-E1C12, BC-E1E10, BC-E1E11…EOQ · Traditional 01/16/2025SE
K242535Single-use Flexible Cystoscope (CY-E2E01, CY-E2E01R, CY-E2F01, CY-E2F01R, CY-E2G01…FAJ · Traditional 12/18/2024SE
K241612Video Bronchoscope System; Single-use Flexible Bronchoscope (BC-S1E00-L, BC-S1H00-L…EOQ · Traditional 10/29/2024SE
K240167Single-use Ureteral Access SheathFED · Traditional 10/08/2024SE
K241434Video Ureteroscope SystemFGB · Special 10/04/2024SE
K230536Single-use Flexible Rhinolaryngoscope; Digital Video MonitorEOB · Traditional 06/14/2023SE

Questions and answers

When was Video Ureteroscope System cleared by the FDA?

Video Ureteroscope System (K231135) received a 510(k) decision of Substantially Equivalent on January 17, 2024, 271 days after the submission was received.

What is the product code of K231135?

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