Biosense Webster, Inc. · Class II · Cleared Jan 6, 2009
| K-number | K081258 |
| Device name | VARIABLE LASSO NAV CATHETER, MODELS: D-1290-01, D-1290-02 |
| Applicant | Biosense Webster, Inc. |
| Product code | DRF |
| Device class | Class II |
| Decision date | Jan 6, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 870.1220 |
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