| K-number | K943143 |
| Device name | BILIARY STENT |
| Applicant | Menlo Care, Inc. |
| Product code | FGE |
| Device class | Class II |
| Decision date | Feb 28, 1995 |
| 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