Abbott Laboratories · Class II · Cleared Dec 10, 2003
| K-number | K033537 |
| Device name | SELFX XPERT BILIARY STENT, MODELS EX8L2005, EX8L3005, EX8L4005, EX8L2006, EX8L3006, EX8L4006, EX8S2005, AND EX8S3005 |
| Applicant | Abbott Laboratories |
| Product code | FGE |
| Device class | Class II |
| Decision date | Dec 10, 2003 |
| 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