K041796 is an FDA 510(k) clearance for the PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM. This device is classified as a Stents, Drains And Dilators For The Biliary Ducts (Class II - Special Controls, product code FGE).
Submitted by Cordis Corporation (Miami Lakes, US). The FDA issued a Cleared decision on August 3, 2004, 32 days after receiving the submission on July 2, 2004.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5010.
| 510(k) Number | K041796 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Abbreviated 510(k) (SESU) |
| Date Received | July 02, 2004 |
| Decision Date | August 03, 2004 |
| Days to Decision | 32 days |
| Submission Type | Special |
| 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 |