Abbott Laboratories · Class II · Cleared Feb 16, 2005
| K-number | K050103 |
| Device name | XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM |
| Applicant | Abbott Laboratories |
| Product code | FGE |
| Device class | Class II |
| Decision date | Feb 16, 2005 |
| Decision | Substantially Equivalent |
| 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