Medtronic Vascular · Class II · Cleared Jun 30, 2023
| K-number | K230156 |
| Device name | 5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter |
| Applicant | Medtronic Vascular |
| Product code | DQY |
| Device class | Class II |
| Decision date | Jun 30, 2023 |
| Decision | Substantially Equivalent |
| Regulation | 870.1250 |
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