Rigid Ureteroscope
FDA 510(k) K901214 · Applied Urology, Inc.
510(k) numberK901214
Submission
- Device name
- Rigid Ureteroscope
- Applicant
- Applied Urology, Inc.
Launa Hills, CA, US - Received
- March 14, 1990
- Decision date
- June 1, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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) | Device | Applicant | Decision |
|---|---|---|---|
| K262488 | Single-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 |
| K261153 | LithoVue Elite Digital Flexible Ureteroscope SystemFGB · Traditional | Boston Scientific Corporation | 08/26/2026SE |
| K262552 | Single-use Flexible Ureteroscope (Single-use Flexible Ureteroscope: SUV-5C-B)FGB · Special | Scivita Medical Technology Co., Ltd. | 08/14/2026SE |
| K253505 | Zamenix PFGB · Traditional | Roen Surgical, Inc. | 08/07/2026SE |
| K260516 | BubbleView Single-Use Digital Flexible Cystoscope (C38-CS, C38-CRS, C50-C, C50-CR…FGB · Traditional | MacroLux Medical Technology Co., Ltd. | 07/20/2026SE |
| K252929 | Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model…FGB · Traditional | Anhui Happiness Workshop Instruments Co., Ltd. | 04/09/2026SE |
| K260013 | CVAC Image ProcessorFGB · Traditional | Calyxo, Inc. | 03/06/2026SE |
| K252468 | Single-use Digital Flexible Ureteroscope (GY-UR9.3); Single-use Digital Flexible…FGB · Traditional | Zhejiang Geyi Medical Instrument Co., Ltd. | 12/16/2025SE |
| K251951 | Single-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 |
| K253411 | Miniature Telescope for Urology (27033AA)FGB · Traditional | Karl Storz SE & CO. KG | 11/18/2025SE |
More from Karl Storz SE & CO. KG
| 510(k) | Device | Decision |
|---|---|---|
| K921838 | Acucise Ureteral Cutting CatheterEYB · Traditional | 02/26/1993SE |
| K925282 | Urological Catheter and AccessoriesFAD · Traditional | 01/13/1993SE |
| K920695 | Ureteral StentFAD · Traditional | 09/23/1992SE |
| K915219 | Urethral Electrode SheathFAS · Traditional | 07/23/1992SE |
| K912093 | Disposable Aspiration Irrigation SystemHET · Traditional | 04/24/1992SE |
| K920030 | Sureseal Endoscopic ValveODC · Traditional | 03/18/1992SE |
| K912656 | Endoscopic ElectrodeGEI · Traditional | 09/16/1991SE |
| K912903 | Percutaneous Retractor KitGCJ · Traditional | 08/16/1991SE |
| K905731 | Flexible Endoscopic ElectrodeFAS · Traditional | 01/31/1991SE |
| K903994 | Ureteropyelogram Cath for Retrograde Dye InjectionFGF · Traditional | 10/19/1990SE |
Questions and answers
When was Rigid Ureteroscope cleared by the FDA?
Rigid Ureteroscope (K901214) received a 510(k) decision of Substantially Equivalent on June 1, 1990, 79 days after the submission was received.
What is the product code of K901214?
The FDA product code is FGB – Ureteroscope And Accessories, Flexible/Rigid, a Class II (moderate risk) device regulated under 21 CFR 876.1500.