Cordis Corp. · Class II · Cleared Mar 23, 2000
| K-number | K000564 |
| Device name | CORDIS MEDIUM PALMAZ TRANSHEPATIC BILIARY STENT & DELIVERY |
| Applicant | Cordis Corp. |
| Product code | FGE |
| Device class | Class II |
| Decision date | Mar 23, 2000 |
| Decision | Unknown |
| Regulation | 876.5010 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov