Medtronic Vascular · Class II · Cleared Dec 4, 2009
| K-number | K091582 |
| Device name | GTX GUIDEWIRE, MODELS TBD-GTX 1, 3,6,9,12, 15 |
| Applicant | Medtronic Vascular |
| Product code | DQX |
| Device class | Class II |
| Decision date | Dec 4, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 870.1330 |
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