K250573 is an FDA 510(k) clearance for the Single Use Cannula V PR-V223Q/V414Q/V416Q/V418Q/V420Q/V427Q/V434Q/V435Q. This device is classified as a Endoscopic Retrograde Cholangiopancreatography (ercp) Cannula (Class II - Special Controls, product code ODD).
Submitted by Olympus Medical Systems Corp. (Hachioji-Shi, JP). The FDA issued a Cleared decision on May 27, 2025, 90 days after receiving the submission on February 26, 2025.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500. To Identify Stones, Tumors, Or Narrowing In The Biliary Tree..
| 510(k) Number | K250573 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 26, 2025 |
| Decision Date | May 27, 2025 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | ODD — Endoscopic Retrograde Cholangiopancreatography (ercp) Cannula |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1500 |
| Definition | To Identify Stones, Tumors, Or Narrowing In The Biliary Tree. |