| K-number | K013150 |
| Device name | MR-GUIDE 2000 |
| Applicant | Ultraguide , Ltd. |
| Product code | LNH |
| Device class | Class II |
| Decision date | Oct 18, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 892.1000 |
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