Disposable Endoscopy Valve Set
FDA 510(k) K250732 · Yangzhou Fartley Medical Instrument Technology Co., Ltd.
510(k) numberK250732
Submission
- Device name
- Disposable Endoscopy Valve Set
- Applicant
- Yangzhou Fartley Medical Instrument Technology Co., Ltd.
Yangzhou, CN - Received
- March 11, 2025
- Decision date
- June 20, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- ODC – Endoscope Channel Accessory
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1500
- Specialty
- Gastroenterology, Urology
To give the endoscope channel additional or improved functionality.
Other 510(k)s with product code ODC
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252933 | Dyne PortODC · Traditional | Dyne Medical Group, Inc. | 06/12/2026SE |
| K250145 | Biopsy Port AdapterODC · Traditional | Endosound, Inc. | 10/17/2025SE |
| K252910 | Orca Air/Water and Suction ValvesODC · Special | Boston Scientific | 10/09/2025SESK |
| K250949 | Suction Valve (MAJ-1443); Air/Water Valve (MAJ-1444)ODC · Traditional | Olympus Medical Systems Corporation | 07/16/2025SE |
| K241842 | Luer-Split MAJ-2092ODC · Traditional | Olympus Medical Systems Corporation | 03/19/2025SE |
| K250140 | Defendo Fujifilm 700 Single Use Cleaning AdapterODC · Special | Steris Corparation | 02/20/2025SE |
| K243075 | Defendo Single Use Cleaning Adapter for Olympus Endoscopes (100322, 100323, 4000096…ODC · Special | STERIS Corporation | 11/08/2024SE |
| K242742 | DEFENDO Single Use Valve Kit AW/S Valves - 2pc for OLYMPUS EUS (00711900)ODC · Special | STERIS Corporation | 10/11/2024SE |
| K241285 | Disposable Endoscope Valves Set (AF series)ODC · Traditional | Alton (Shanghai) Medical Instruments Co., Ltd. | 10/01/2024SE |
| K232067 | Defendo Fujifilm 500/600 Single Use Air/Water Valve, Defendo Fujifilm 500/600 Single Use…ODC · Traditional | Medivators (A Subsidiary of Steris Corporation) | 03/22/2024SE |
More from Medivators (A Subsidiary of Steris Corporation)
| 510(k) | Device | Decision |
|---|---|---|
| K260423 | Disposable Endoscopic Distal AttachmentsFDF · Traditional | 05/28/2026SE |
| K230004 | Disposable HemoclipPKL · Traditional | 07/31/2023SE |
| K222980 | Pentax Medical Valve SetODC · Traditional | 11/21/2022SE |
| K220785 | Clean Connecting TubeOCX · Traditional | 09/27/2022SE |
| K220292 | Disposable Endoscope Injection NeedleFBK · Traditional | 08/19/2022SE |
| K220790 | Disposable Polypectomy Snare, Disposable Polypectomy Hybrid SnareFDI · Traditional | 06/27/2022SE |
| K220210 | Disposable Endoscopy Adapter SetODC · Traditional | 06/17/2022SE |
Questions and answers
When was Disposable Endoscopy Valve Set cleared by the FDA?
Disposable Endoscopy Valve Set (K250732) received a 510(k) decision of Substantially Equivalent on June 20, 2025, 101 days after the submission was received.
What is the product code of K250732?
The FDA product code is ODC – Endoscope Channel Accessory, a Class II (moderate risk) device regulated under 21 CFR 876.1500.