K241888 is an FDA 510(k) clearance for the Single-use Balloon Dilatation Catheter, a Stents, Drains And Dilators For The Biliary Ducts (Class II — Special Controls, product code FGE), submitted by Leo Medical Co., Ltd. (Changzhou, CN). The FDA issued a Cleared decision on December 20, 2024, 175 days after receiving the submission on June 28, 2024. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5010.
| 510(k) Number | K241888 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 28, 2024 |
| Decision Date | December 20, 2024 |
| Days to Decision | 175 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FGE — Stents, Drains And Dilators For The Biliary Ducts |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.5010 |