C.R. Bard, Inc. · Class II · Cleared Apr 2, 2002
| K-number | K020682 |
| Device name | BARD LUMINEXX 6 FR BILIARY STENT AND DELIVERY SYSTEM |
| Applicant | C.R. Bard, Inc. |
| Product code | FGE |
| Device class | Class II |
| Decision date | Apr 2, 2002 |
| 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