Medtronic, Ireland · Class II · Cleared Oct 29, 2025
| K-number | K252390 |
| Device name | Telescope Guide Extension Catheter |
| Applicant | Medtronic, Ireland |
| Product code | DQY |
| Device class | Class II |
| Decision date | Oct 29, 2025 |
| Decision | Substantially Equivalent |
| Regulation | 870.1250 |
The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →
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