Cordis Corporation · Class II · Cleared Aug 3, 2004
| K-number | K041796 |
| Device name | PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM |
| Applicant | Cordis Corporation |
| Product code | FGE |
| Device class | Class II |
| Decision date | Aug 3, 2004 |
| Decision | Unknown |
| Regulation | 876.5010 |
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