K250128 is an FDA 510(k) clearance for the Single Use Suction-Evacuation Ureteral Access Sheath, a Endoscopic Access Overtube, Gastroenterology-urology (Class II — Special Controls, product code FED), submitted by Anhui Happiness Workshop Medical Instruments Co., Ltd. (Bengbu, CN). The FDA issued a Cleared decision on September 19, 2025, 245 days after receiving the submission on January 17, 2025. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K250128 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 17, 2025 |
| Decision Date | September 19, 2025 |
| Days to Decision | 245 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FED — Endoscopic Access Overtube, Gastroenterology-urology |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1500 |
| Definition | To Facilitate Passage And Aid Advancement Of Endoscopes Into The Body, Especially In Cases Of Repeated Intubation. |